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nsv5478685

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,582

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 27 studies. See in: genome view    
Submitted genomic138,802,270-138,803,851Question Mark
Overlapping variant regions from other studies: 120 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):138,487,015-138,488,596Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5478685Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7138,802,270138,803,851
nsv5478685RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7138,487,015138,488,596

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17006307duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17006307Submitted genomicNC_000007.14:g.138
802270_138803851du
p
GRCh38 (hg38)NC_000007.14Chr7138,802,270138,803,851
nssv17006307RemappedPerfectNC_000007.13:g.138
487015_138488596du
p
GRCh37.p13First PassNC_000007.13Chr7138,487,015138,488,596

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)
nssv17006307<0.00116404
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