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nsv5479126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 37 studies. See in: genome view    
Submitted genomic100,024,652-100,024,773Question Mark
Overlapping variant regions from other studies: 140 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):99,622,275-99,622,396Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,024,652100,024,773
nsv5479126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,622,27599,622,396

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002937deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002937Submitted genomicNC_000007.14:g.100
024652_100024773de
l
GRCh38 (hg38)NC_000007.14Chr7100,024,652100,024,773
nssv17002937RemappedPerfectNC_000007.13:g.996
22275_99622396del
GRCh37.p13First PassNC_000007.13Chr799,622,27599,622,396

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)
nssv17002937<0.00116404
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