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nsv5512678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 23 studies. See in: genome view    
Submitted genomic46,785,576-46,785,669Question Mark
Overlapping variant regions from other studies: 79 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):47,179,359-47,179,452Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1246,785,57646,785,669
nsv5512678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1247,179,35947,179,452

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056754duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056754Submitted genomicNC_000012.12:g.467
85576_46785669dup
GRCh38 (hg38)NC_000012.12Chr1246,785,57646,785,669
nssv17056754RemappedPerfectNC_000012.11:g.471
79359_47179452dup
GRCh37.p13First PassNC_000012.11Chr1247,179,35947,179,452

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)
nssv17056754<0.00116404
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