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esv2761959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:243,642

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1307 SVs from 91 studies. See in: genome view    
Remapped(Score: Good):43,322,294-43,565,935Question Mark
Overlapping variant regions from other studies: 1341 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):41,399,657-41,643,303Question Mark
Overlapping variant regions from other studies: 360 SVs from 28 studies. See in: genome view    
Submitted genomic38,755,183-38,998,829Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2761959RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1743,322,29443,565,935
esv2761959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,399,65741,643,303
esv2761959Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000017.9Chr1738,755,18338,998,829

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7002143copy number gainSW_0885SNP arraySNP genotyping analysis50

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7002143RemappedGoodNC_000017.11:g.(?_
43322294)_(4356593
5_?)dup
GRCh38.p12First PassNC_000017.11Chr1743,322,29443,565,935
essv7002143RemappedPerfectNC_000017.10:g.(?_
41399657)_(4164330
3_?)dup
GRCh37.p13First PassNC_000017.10Chr1741,399,65741,643,303
essv7002143Submitted genomicNC_000017.9:g.(?_3
8755183)_(38998829
_?)dup
NCBI36 (hg18)NC_000017.9Chr1738,755,18338,998,829

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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