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esv12565

  • Variant Calls:9
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:37,660

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 592 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):10,413,490-10,451,149Question Mark
Overlapping variant regions from other studies: 593 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):10,566,089-10,603,748Question Mark
Overlapping variant regions from other studies: 212 SVs from 26 studies. See in: genome view    
Submitted genomic10,457,356-10,495,015Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv12565RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1210,413,49010,451,149
esv12565RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,566,08910,603,748
esv12565Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1210,457,35610,495,015

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv46494copy number lossNA19129Oligo aCGHProbe signal intensity1,564
essv54992copy number lossNA19099Oligo aCGHProbe signal intensity1,498
essv61985copy number lossNA12239Oligo aCGHProbe signal intensity1,252
essv49726copy number lossNA18517Oligo aCGHProbe signal intensity1,365
essv76352copy number lossNA12414Oligo aCGHProbe signal intensity1,122
essv82362copy number lossNA19114Oligo aCGHProbe signal intensity1,473
essv58989copy number lossNA19108Oligo aCGHProbe signal intensity1,563
essv79352copy number lossNA12749Oligo aCGHProbe signal intensity1,232
essv32326copy number lossNA19147Oligo aCGHProbe signal intensity1,541

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv46494RemappedPerfectNC_000012.12:g.(?_
10413490)_(1044679
8_?)del		GRCh38.p12First PassNC_000012.12Chr1210,413,49010,446,798
essv54992RemappedPerfectNC_000012.12:g.(?_
10414458)_(1044636
0_?)del		GRCh38.p12First PassNC_000012.12Chr1210,414,45810,446,360
essv61985RemappedPerfectNC_000012.12:g.(?_
10416563)_(1044363
7_?)del		GRCh38.p12First PassNC_000012.12Chr1210,416,56310,443,637
essv49726RemappedPerfectNC_000012.12:g.(?_
10416659)_(1044642
3_?)del		GRCh38.p12First PassNC_000012.12Chr1210,416,65910,446,423
essv76352RemappedPerfectNC_000012.12:g.(?_
10416732)_(1044664
5_?)del		GRCh38.p12First PassNC_000012.12Chr1210,416,73210,446,645
essv82362RemappedPerfectNC_000012.12:g.(?_
10416732)_(1044679
8_?)del		GRCh38.p12First PassNC_000012.12Chr1210,416,73210,446,798
essv58989RemappedPerfectNC_000012.12:g.(?_
10416732)_(1045114
9_?)del		GRCh38.p12First PassNC_000012.12Chr1210,416,73210,451,149
essv79352RemappedPerfectNC_000012.12:g.(?_
10418472)_(1044449
8_?)del		GRCh38.p12First PassNC_000012.12Chr1210,418,47210,444,498
essv32326RemappedPerfectNC_000012.12:g.(?_
10418807)_(1044620
0_?)del		GRCh38.p12First PassNC_000012.12Chr1210,418,80710,446,200
essv46494RemappedPerfectNC_000012.11:g.(?_
10566089)_(1059939
7_?)del		GRCh37.p13First PassNC_000012.11Chr1210,566,08910,599,397
essv54992RemappedPerfectNC_000012.11:g.(?_
10567057)_(1059895
9_?)del		GRCh37.p13First PassNC_000012.11Chr1210,567,05710,598,959
essv61985RemappedPerfectNC_000012.11:g.(?_
10569162)_(1059623
6_?)del		GRCh37.p13First PassNC_000012.11Chr1210,569,16210,596,236
essv49726RemappedPerfectNC_000012.11:g.(?_
10569258)_(1059902
2_?)del		GRCh37.p13First PassNC_000012.11Chr1210,569,25810,599,022
essv76352RemappedPerfectNC_000012.11:g.(?_
10569331)_(1059924
4_?)del		GRCh37.p13First PassNC_000012.11Chr1210,569,33110,599,244
essv82362RemappedPerfectNC_000012.11:g.(?_
10569331)_(1059939
7_?)del		GRCh37.p13First PassNC_000012.11Chr1210,569,33110,599,397
essv58989RemappedPerfectNC_000012.11:g.(?_
10569331)_(1060374
8_?)del		GRCh37.p13First PassNC_000012.11Chr1210,569,33110,603,748
essv79352RemappedPerfectNC_000012.11:g.(?_
10571071)_(1059709
7_?)del		GRCh37.p13First PassNC_000012.11Chr1210,571,07110,597,097
essv32326RemappedPerfectNC_000012.11:g.(?_
10571406)_(1059879
9_?)del		GRCh37.p13First PassNC_000012.11Chr1210,571,40610,598,799
essv46494Submitted genomicNC_000012.10:g.(?_
10457356)_(1049066
4_?)del		NCBI36 (hg18)NC_000012.10Chr1210,457,35610,490,664
essv54992Submitted genomicNC_000012.10:g.(?_
10458324)_(1049022
6_?)del		NCBI36 (hg18)NC_000012.10Chr1210,458,32410,490,226
essv61985Submitted genomicNC_000012.10:g.(?_
10460429)_(1048750
3_?)del		NCBI36 (hg18)NC_000012.10Chr1210,460,42910,487,503
essv49726Submitted genomicNC_000012.10:g.(?_
10460525)_(1049028
9_?)del		NCBI36 (hg18)NC_000012.10Chr1210,460,52510,490,289
essv76352Submitted genomicNC_000012.10:g.(?_
10460598)_(1049051
1_?)del		NCBI36 (hg18)NC_000012.10Chr1210,460,59810,490,511
essv82362Submitted genomicNC_000012.10:g.(?_
10460598)_(1049066
4_?)del		NCBI36 (hg18)NC_000012.10Chr1210,460,59810,490,664
essv58989Submitted genomicNC_000012.10:g.(?_
10460598)_(1049501
5_?)del		NCBI36 (hg18)NC_000012.10Chr1210,460,59810,495,015
essv79352Submitted genomicNC_000012.10:g.(?_
10462338)_(1048836
4_?)del		NCBI36 (hg18)NC_000012.10Chr1210,462,33810,488,364
essv32326Submitted genomicNC_000012.10:g.(?_
10462673)_(1049006
6_?)del		NCBI36 (hg18)NC_000012.10Chr1210,462,67310,490,066

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv619852NA12239Oligo aCGHProbe signal intensityPass
essv763522NA12414Oligo aCGHProbe signal intensityPass
essv793522NA12749Oligo aCGHProbe signal intensityPass
essv497262NA18517Oligo aCGHProbe signal intensityPass
essv549922NA19099Oligo aCGHProbe signal intensityPass
essv589892NA19108Oligo aCGHProbe signal intensityPass
essv823622NA19114Oligo aCGHProbe signal intensityPass
essv464942NA19129Oligo aCGHProbe signal intensityPass
essv323262NA19147Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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