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esv3892279

  • Variant Calls:34
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,725

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 647 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):131,313,063-131,345,787Question Mark
Overlapping variant regions from other studies: 647 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):131,797,608-131,830,332Question Mark
Overlapping variant regions from other studies: 245 SVs from 26 studies. See in: genome view    
Submitted genomic130,363,561-130,396,285Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3892279RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12131,313,063131,315,514131,331,668131,345,787
esv3892279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12131,797,608131,800,059131,816,213131,830,332
esv3892279Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr12130,363,561130,366,012130,382,166130,396,285

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
essv25782618copy number lossSNP arrayProbe signal intensity1
essv25797345copy number lossSNP arrayProbe signal intensity1
essv25797358copy number lossSNP arrayProbe signal intensity1
essv25798017copy number lossSNP arrayProbe signal intensity1
essv25798553copy number lossSNP arrayProbe signal intensity1
essv25778913copy number lossSNP arrayProbe signal intensity1
essv25778959copy number lossSNP arrayProbe signal intensity1
essv25779700copy number lossSNP arrayProbe signal intensity1
essv25779782copy number lossSNP arrayProbe signal intensity1
essv25780088copy number lossSNP arrayProbe signal intensity1
essv25782465copy number lossSNP arrayProbe signal intensity1
essv25783246copy number lossSNP arrayProbe signal intensity1
essv25783321copy number lossSNP arrayProbe signal intensity1
essv25783733copy number lossSNP arrayProbe signal intensity1
essv25784181copy number lossSNP arrayProbe signal intensity1
essv25784639copy number lossSNP arrayProbe signal intensity1
essv25784945copy number lossSNP arrayProbe signal intensity1
essv25785927copy number lossSNP arrayProbe signal intensity1
essv25786214copy number lossSNP arrayProbe signal intensity1
essv25786295copy number lossSNP arrayProbe signal intensity1
essv25786871copy number lossSNP arrayProbe signal intensity1
essv25787341copy number lossSNP arrayProbe signal intensity1
essv25787471copy number lossSNP arrayProbe signal intensity1
essv25796181copy number lossSNP arrayProbe signal intensity1
essv25797121copy number lossSNP arrayProbe signal intensity1
essv25797898copy number lossSNP arrayProbe signal intensity1
essv25799413copy number lossSNP arrayProbe signal intensity1
essv25800432copy number lossSNP arrayProbe signal intensity1
essv25800526copy number lossSNP arrayProbe signal intensity1
essv25800973copy number lossSNP arrayProbe signal intensity1
essv25792963copy number gainSNP arrayProbe signal intensity3
essv25783545copy number lossSNP arrayProbe signal intensity1
essv25783762copy number lossSNP arrayProbe signal intensity1
essv25800912copy number lossSNP arrayProbe signal intensity1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv25782618RemappedPerfectNC_000012.12:g.(?_
131313063)_(131331
668_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,331,668
essv25797345RemappedPerfectNC_000012.12:g.(?_
131313063)_(131331
668_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,331,668
essv25797358RemappedPerfectNC_000012.12:g.(?_
131313063)_(131331
668_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,331,668
essv25798017RemappedPerfectNC_000012.12:g.(?_
131313063)_(131331
668_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,331,668
essv25798553RemappedPerfectNC_000012.12:g.(?_
131313063)_(131331
668_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,331,668
essv25778913RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25778959RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25779700RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25779782RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25780088RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25782465RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25783246RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25783321RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25783733RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25784181RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25784639RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25784945RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25785927RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25786214RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25786295RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25786871RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25787341RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25787471RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25796181RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25797121RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25797898RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25799413RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25800432RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25800526RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25800973RemappedPerfectNC_000012.12:g.(?_
131313063)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,340,251
essv25792963RemappedPerfectNC_000012.12:g.(?_
131313063)_(131345
787_?)dup
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,345,787
essv25783545RemappedPerfectNC_000012.12:g.(?_
131315514)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,315,514131,340,251
essv25783762RemappedPerfectNC_000012.12:g.(?_
131315514)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,315,514131,340,251
essv25800912RemappedPerfectNC_000012.12:g.(?_
131315514)_(131340
251_?)del
GRCh38.p12First PassNC_000012.12Chr12131,315,514131,340,251
essv25782618RemappedPerfectNC_000012.11:g.(?_
131797608)_(131816
213_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,816,213
essv25797345RemappedPerfectNC_000012.11:g.(?_
131797608)_(131816
213_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,816,213
essv25797358RemappedPerfectNC_000012.11:g.(?_
131797608)_(131816
213_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,816,213
essv25798017RemappedPerfectNC_000012.11:g.(?_
131797608)_(131816
213_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,816,213
essv25798553RemappedPerfectNC_000012.11:g.(?_
131797608)_(131816
213_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,816,213
essv25778913RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25778959RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25779700RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25779782RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25780088RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25782465RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25783246RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25783321RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25783733RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25784181RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25784639RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25784945RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25785927RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25786214RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25786295RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25786871RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25787341RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25787471RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25796181RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25797121RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25797898RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25799413RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25800432RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25800526RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25800973RemappedPerfectNC_000012.11:g.(?_
131797608)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,824,796
essv25792963RemappedPerfectNC_000012.11:g.(?_
131797608)_(131830
332_?)dup
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,830,332
essv25783545RemappedPerfectNC_000012.11:g.(?_
131800059)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,800,059131,824,796
essv25783762RemappedPerfectNC_000012.11:g.(?_
131800059)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,800,059131,824,796
essv25800912RemappedPerfectNC_000012.11:g.(?_
131800059)_(131824
796_?)del
GRCh37.p13First PassNC_000012.11Chr12131,800,059131,824,796
essv25782618Submitted genomicNC_000012.10:g.(?_
130363561)_(130382
166_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,382,166
essv25797345Submitted genomicNC_000012.10:g.(?_
130363561)_(130382
166_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,382,166
essv25797358Submitted genomicNC_000012.10:g.(?_
130363561)_(130382
166_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,382,166
essv25798017Submitted genomicNC_000012.10:g.(?_
130363561)_(130382
166_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,382,166
essv25798553Submitted genomicNC_000012.10:g.(?_
130363561)_(130382
166_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,382,166
essv25778913Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25778959Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25779700Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25779782Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25780088Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25782465Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25783246Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25783321Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25783733Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25784181Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25784639Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25784945Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25785927Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25786214Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25786295Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25786871Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25787341Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25787471Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25796181Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25797121Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25797898Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25799413Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25800432Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25800526Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25800973Submitted genomicNC_000012.10:g.(?_
130363561)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,390,749
essv25792963Submitted genomicNC_000012.10:g.(?_
130363561)_(130396
285_?)dup
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,396,285
essv25783545Submitted genomicNC_000012.10:g.(?_
130366012)_(130390
749_?)del
NCBI36 (hg18)NC_000012.10Chr12130,366,012130,390,749
Showing 100 of 102

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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