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nsv5483050

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:326,976

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1594 SVs from 86 studies. See in: genome view    
Submitted genomic27,042,537-27,369,512Question Mark
Overlapping variant regions from other studies: 1594 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):27,331,466-27,658,441Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1027,042,53727,369,512
nsv5483050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1027,331,46627,658,441

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17033288duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17033288Submitted genomicNC_000010.11:g.270
42537_27369512dup
GRCh38 (hg38)NC_000010.11Chr1027,042,53727,369,512
nssv17033288RemappedPerfectNC_000010.10:g.273
31466_27658441dup
GRCh37.p13First PassNC_000010.10Chr1027,331,46627,658,441

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)
nssv17033288<0.00116404
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