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nsv5465523

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,640,677

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 6898 SVs from 114 studies. See in: genome view    
Submitted genomic177,669,324-179,310,000Question Mark
Overlapping variant regions from other studies: 6898 SVs from 114 studies. See in: genome view    
Remapped(Score: Perfect):177,096,325-178,737,001Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465523Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5177,669,324179,310,000
nsv5465523RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5177,096,325178,737,001

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16976828duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16976828Submitted genomicNC_000005.10:g.177
669324_179310000du
p
GRCh38 (hg38)NC_000005.10Chr5177,669,324179,310,000
nssv16976828RemappedPerfectNC_000005.9:g.1770
96325_178737001dup
GRCh37.p13First PassNC_000005.9Chr5177,096,325178,737,001

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)
nssv16976828<0.00116404
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