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nsv5469534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 67 SVs from 18 studies. See in: genome view    
Submitted genomic175,681,327-175,681,413Question Mark
Overlapping variant regions from other studies: 67 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):175,108,330-175,108,416Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5469534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5175,681,327175,681,413
nsv5469534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5175,108,330175,108,416

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978708duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978708Submitted genomicNC_000005.10:g.175
681327_175681413du
p
GRCh38 (hg38)NC_000005.10Chr5175,681,327175,681,413
nssv16978708RemappedPerfectNC_000005.9:g.1751
08330_175108416dup
GRCh37.p13First PassNC_000005.9Chr5175,108,330175,108,416

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)
nssv16978708<0.00116404
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