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nsv820358

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 722 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):152,256,301-152,293,321Question Mark
Overlapping variant regions from other studies: 733 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):151,953,386-151,990,406Question Mark
Overlapping variant regions from other studies: 255 SVs from 21 studies. See in: genome view    
Submitted genomic151,584,319-151,621,339Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv820358RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7152,256,301152,293,321
nsv820358RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7151,953,386151,990,406
nsv820358Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr7151,584,319151,621,339

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1420707duplicationNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1420707RemappedPerfectNC_000007.14:g.(?_
152256301)_(152293
321_?)dup
GRCh38.p12First PassNC_000007.14Chr7152,256,301152,293,321
nssv1420707RemappedPerfectNC_000007.13:g.(?_
151953386)_(151990
406_?)dup
GRCh37.p13First PassNC_000007.13Chr7151,953,386151,990,406
nssv1420707Submitted genomicNC_000007.12:g.(?_
151584319)_(151621
339_?)dup
NCBI36 (hg18)NC_000007.12Chr7151,584,319151,621,339

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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