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nsv5896676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 206 SVs from 38 studies. See in: genome view    
Submitted genomic131,607,047-131,607,192Question Mark
Overlapping variant regions from other studies: 206 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):132,364,620-132,364,765Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5896676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,607,047131,607,192
nsv5896676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,364,620132,364,765

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17398113duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17398113Submitted genomicNC_000002.12:g.131
607047_131607192du
p
GRCh38 (hg38)NC_000002.12Chr2131,607,047131,607,192
nssv17398113RemappedPerfectNC_000002.11:g.132
364620_132364765du
p
GRCh37.p13First PassNC_000002.11Chr2132,364,620132,364,765

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)
nssv173981130.00111692
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