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nsv5486761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,184

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 215 SVs from 47 studies. See in: genome view    
Submitted genomic42,705,332-42,753,515Question Mark
Overlapping variant regions from other studies: 211 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):43,200,780-43,248,963Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1042,705,33242,753,515
nsv5486761RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1043,200,78043,248,963

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17033530duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17033530Submitted genomicNC_000010.11:g.427
05332_42753515dup
GRCh38 (hg38)NC_000010.11Chr1042,705,33242,753,515
nssv17033530RemappedPerfectNC_000010.10:g.432
00780_43248963dup
GRCh37.p13First PassNC_000010.10Chr1043,200,78043,248,963

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)
nssv17033530<0.00136404
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