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nsv5483036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:393,693

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1025 SVs from 76 studies. See in: genome view    
Submitted genomic103,668,884-104,062,576Question Mark
Overlapping variant regions from other studies: 1025 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):103,309,331-103,703,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7103,668,884104,062,576
nsv5483036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7103,309,331103,703,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17000604duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17000604Submitted genomicNC_000007.14:g.103
668884_104062576du
p
GRCh38 (hg38)NC_000007.14Chr7103,668,884104,062,576
nssv17000604RemappedPerfectNC_000007.13:g.103
309331_103703023du
p
GRCh37.p13First PassNC_000007.13Chr7103,309,331103,703,023

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)
nssv17000604<0.00116404
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