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nsv5511928

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379,725

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1464 SVs from 95 studies. See in: genome view    
Submitted genomic42,914,564-43,294,288Question Mark
Overlapping variant regions from other studies: 1464 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):43,488,700-43,868,424Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5511928Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1342,914,56443,294,288
nsv5511928RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,488,70043,868,424

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687252duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687252Submitted genomicNC_000013.11:g.429
14564_43294288dup
GRCh38 (hg38)NC_000013.11Chr1342,914,56443,294,288
nssv17687252RemappedPerfectNC_000013.10:g.434
88700_43868424dup
GRCh37.p13First PassNC_000013.10Chr1343,488,70043,868,424

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)
nssv17687252<0.00156404
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