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esv2761170

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,634

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 277 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):18,176,663-18,179,296Question Mark
Overlapping variant regions from other studies: 277 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):18,034,172-18,036,805Question Mark
Overlapping variant regions from other studies: 142 SVs from 10 studies. See in: genome view    
Submitted genomic18,078,452-18,081,085Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2761170RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr818,176,66318,179,296
esv2761170RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr818,034,17218,036,805
esv2761170Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr818,078,45218,081,085

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7016514copy number lossRW_0204SNP arraySNP genotyping analysis40
essv7016515copy number lossRW_0653SNP arraySNP genotyping analysis55
essv7016516copy number lossRW_0211SNP arraySNP genotyping analysis62

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7016514RemappedPerfectNC_000008.11:g.(?_
18176663)_(1817929
6_?)del
GRCh38.p12First PassNC_000008.11Chr818,176,66318,179,296
essv7016515RemappedPerfectNC_000008.11:g.(?_
18176663)_(1817929
6_?)del
GRCh38.p12First PassNC_000008.11Chr818,176,66318,179,296
essv7016516RemappedPerfectNC_000008.11:g.(?_
18177517)_(1817929
6_?)del
GRCh38.p12First PassNC_000008.11Chr818,177,51718,179,296
essv7016514RemappedPerfectNC_000008.10:g.(?_
18034172)_(1803680
5_?)del
GRCh37.p13First PassNC_000008.10Chr818,034,17218,036,805
essv7016515RemappedPerfectNC_000008.10:g.(?_
18034172)_(1803680
5_?)del
GRCh37.p13First PassNC_000008.10Chr818,034,17218,036,805
essv7016516RemappedPerfectNC_000008.10:g.(?_
18035026)_(1803680
5_?)del
GRCh37.p13First PassNC_000008.10Chr818,035,02618,036,805
essv7016514Submitted genomicNC_000008.9:g.(?_1
8078452)_(18081085
_?)del
NCBI36 (hg18)NC_000008.9Chr818,078,45218,081,085
essv7016515Submitted genomicNC_000008.9:g.(?_1
8078452)_(18081085
_?)del
NCBI36 (hg18)NC_000008.9Chr818,078,45218,081,085
essv7016516Submitted genomicNC_000008.9:g.(?_1
8079306)_(18081085
_?)del
NCBI36 (hg18)NC_000008.9Chr818,079,30618,081,085

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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