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nsv5485762

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Submitted genomic137,988,274-137,988,419Question Mark
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):137,673,020-137,673,165Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485762Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7137,988,274137,988,419
nsv5485762RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7137,673,020137,673,165

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003712duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003712Submitted genomicNC_000007.14:g.137
988274_137988419du
p
GRCh38 (hg38)NC_000007.14Chr7137,988,274137,988,419
nssv17003712RemappedPerfectNC_000007.13:g.137
673020_137673165du
p
GRCh37.p13First PassNC_000007.13Chr7137,673,020137,673,165

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)
nssv17003712<0.00116404
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