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nsv5905345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,197

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 651 SVs from 72 studies. See in: genome view    
Submitted genomic97,669,161-97,845,357Question Mark
Overlapping variant regions from other studies: 651 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):98,590,312-98,766,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5905345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr497,669,16197,845,357
nsv5905345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr498,590,31298,766,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17414438duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17414438Submitted genomicNC_000004.12:g.976
69161_97845357dup
GRCh38 (hg38)NC_000004.12Chr497,669,16197,845,357
nssv17414438RemappedPerfectNC_000004.11:g.985
90312_98766508dup
GRCh37.p13First PassNC_000004.11Chr498,590,31298,766,508

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)
nssv174144380.00111812
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