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esv2763660

  • Variant Calls:30
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:131,860

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 737 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):30,185,676-30,317,535Question Mark
Overlapping variant regions from other studies: 724 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):29,420,352-29,552,211Question Mark
Overlapping variant regions from other studies: 182 SVs from 22 studies. See in: genome view    
Submitted genomic28,034,013-28,165,872Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2763660RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2030,185,67630,317,535
esv2763660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2029,420,35229,552,211
esv2763660Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000020.9Chr2028,034,01328,165,872

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7004043copy number lossSW_0002SNP arraySNP genotyping analysis26
essv7004045copy number lossSW_0636SNP arraySNP genotyping analysis31
essv7004046copy number lossSW_0857SNP arraySNP genotyping analysis33
essv7004047copy number lossSW_0888SNP arraySNP genotyping analysis49
essv7004048copy number lossSW_1062SNP arraySNP genotyping analysis33
essv7004049copy number lossSW_1126SNP arraySNP genotyping analysis46
essv7004050copy number lossSW_0786SNP arraySNP genotyping analysis48
essv7004051copy number lossSW_0884SNP arraySNP genotyping analysis33
essv7004052copy number lossSW_0230SNP arraySNP genotyping analysis21
essv7004053copy number lossSW_0253SNP arraySNP genotyping analysis28
essv7004054copy number lossSW_0648SNP arraySNP genotyping analysis41
essv7004056copy number lossSW_0677SNP arraySNP genotyping analysis32
essv7004057copy number lossSW_0813SNP arraySNP genotyping analysis46
essv7004058copy number lossSW_0841SNP arraySNP genotyping analysis37
essv7004059copy number lossSW_0889SNP arraySNP genotyping analysis27
essv7004060copy number lossSW_1065SNP arraySNP genotyping analysis28
essv7004061copy number lossSW_1083SNP arraySNP genotyping analysis29
essv7004062copy number lossSW_1114SNP arraySNP genotyping analysis29
essv7004063copy number lossSW_1172SNP arraySNP genotyping analysis43
essv7004064copy number lossSW_1184SNP arraySNP genotyping analysis41
essv7004065copy number lossSW_1232SNP arraySNP genotyping analysis40
essv7004067copy number lossSW_1244SNP arraySNP genotyping analysis36
essv7004068copy number lossSW_1249SNP arraySNP genotyping analysis41
essv7004069copy number lossSW_1076SNP arraySNP genotyping analysis27
essv7004070copy number lossSW_0872SNP arraySNP genotyping analysis44
essv7004071copy number lossSW_0759SNP arraySNP genotyping analysis44
essv7004072copy number lossSW_1111SNP arraySNP genotyping analysis52
essv7004073copy number lossSW_1080SNP arraySNP genotyping analysis35
essv7004074copy number lossSW_1003SNP arraySNP genotyping analysis34
essv7004075copy number lossSW_1042SNP arraySNP genotyping analysis33

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7004043RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004045RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004046RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004047RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004048RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004049RemappedPerfectNC_000020.11:g.(?_
30185676)_(3025917
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,259,177
essv7004050RemappedPerfectNC_000020.11:g.(?_
30185676)_(3026359
5_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,263,595
essv7004051RemappedPerfectNC_000020.11:g.(?_
30185676)_(3026359
5_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,263,595
essv7004052RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004053RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004054RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004056RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004057RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004058RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004059RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004060RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004061RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004062RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004063RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004064RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004065RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004067RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004068RemappedPerfectNC_000020.11:g.(?_
30185676)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,271,217
essv7004069RemappedPerfectNC_000020.11:g.(?_
30185676)_(3031753
5_?)del
GRCh38.p12First PassNC_000020.11Chr2030,185,67630,317,535
essv7004070RemappedPerfectNC_000020.11:g.(?_
30202126)_(3026359
5_?)del
GRCh38.p12First PassNC_000020.11Chr2030,202,12630,263,595
essv7004071RemappedPerfectNC_000020.11:g.(?_
30202126)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,202,12630,271,217
essv7004072RemappedPerfectNC_000020.11:g.(?_
30202126)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,202,12630,271,217
essv7004073RemappedPerfectNC_000020.11:g.(?_
30202528)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,202,52830,271,217
essv7004074RemappedPerfectNC_000020.11:g.(?_
30245164)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,245,16430,271,217
essv7004075RemappedPerfectNC_000020.11:g.(?_
30245164)_(3027121
7_?)del
GRCh38.p12First PassNC_000020.11Chr2030,245,16430,271,217
essv7004043RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004045RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004046RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004047RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004048RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004049RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949385
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,493,853
essv7004050RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949827
1_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,498,271
essv7004051RemappedPerfectNC_000020.10:g.(?_
29420352)_(2949827
1_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,498,271
essv7004052RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004053RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004054RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004056RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004057RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004058RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004059RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004060RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004061RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004062RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004063RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004064RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004065RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004067RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004068RemappedPerfectNC_000020.10:g.(?_
29420352)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,505,893
essv7004069RemappedPerfectNC_000020.10:g.(?_
29420352)_(2955221
1_?)del
GRCh37.p13First PassNC_000020.10Chr2029,420,35229,552,211
essv7004070RemappedPerfectNC_000020.10:g.(?_
29436802)_(2949827
1_?)del
GRCh37.p13First PassNC_000020.10Chr2029,436,80229,498,271
essv7004071RemappedPerfectNC_000020.10:g.(?_
29436802)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,436,80229,505,893
essv7004072RemappedPerfectNC_000020.10:g.(?_
29436802)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,436,80229,505,893
essv7004073RemappedPerfectNC_000020.10:g.(?_
29437204)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,437,20429,505,893
essv7004074RemappedPerfectNC_000020.10:g.(?_
29479840)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,479,84029,505,893
essv7004075RemappedPerfectNC_000020.10:g.(?_
29479840)_(2950589
3_?)del
GRCh37.p13First PassNC_000020.10Chr2029,479,84029,505,893
essv7004043Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004045Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004046Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004047Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004048Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004049Submitted genomicNC_000020.9:g.(?_2
8034013)_(28107514
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,107,514
essv7004050Submitted genomicNC_000020.9:g.(?_2
8034013)_(28111932
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,111,932
essv7004051Submitted genomicNC_000020.9:g.(?_2
8034013)_(28111932
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,111,932
essv7004052Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004053Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004054Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004056Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004057Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004058Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004059Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004060Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004061Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004062Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004063Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004064Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004065Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004067Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004068Submitted genomicNC_000020.9:g.(?_2
8034013)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,119,554
essv7004069Submitted genomicNC_000020.9:g.(?_2
8034013)_(28165872
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,034,01328,165,872
essv7004070Submitted genomicNC_000020.9:g.(?_2
8050463)_(28111932
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,050,46328,111,932
essv7004071Submitted genomicNC_000020.9:g.(?_2
8050463)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,050,46328,119,554
essv7004072Submitted genomicNC_000020.9:g.(?_2
8050463)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,050,46328,119,554
essv7004073Submitted genomicNC_000020.9:g.(?_2
8050865)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,050,86528,119,554
essv7004074Submitted genomicNC_000020.9:g.(?_2
8093501)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,093,50128,119,554
essv7004075Submitted genomicNC_000020.9:g.(?_2
8093501)_(28119554
_?)del
NCBI36 (hg18)NC_000020.9Chr2028,093,50128,119,554

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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