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nsv2815901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,329

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 568 SVs from 86 studies. See in: genome view    
Submitted genomic134,100,249-134,113,577Question Mark
Overlapping variant regions from other studies: 568 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):133,785,002-133,798,330Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2815901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7134,100,249134,113,577
nsv2815901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7133,785,002133,798,330

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13707414deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13707414Submitted genomicNC_000007.14:g.134
100249_134113577de
l13329
GRCh38 (hg38)NC_000007.14Chr7134,100,249134,113,577
nssv13707414RemappedPerfectNC_000007.13:g.133
785002_133798330de
l13329
GRCh37.p13First PassNC_000007.13Chr7133,785,002133,798,330

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv137074140.2971964
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