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nsv5435461

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,383

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 588 SVs from 71 studies. See in: genome view    
Submitted genomic131,259,618-131,332,000Question Mark
Overlapping variant regions from other studies: 588 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):132,017,191-132,089,573Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5435461Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,259,618131,332,000
nsv5435461RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,017,191132,089,573

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16919235duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16919235Submitted genomicNC_000002.12:g.131
259618_131332000du
p
GRCh38 (hg38)NC_000002.12Chr2131,259,618131,332,000
nssv16919235RemappedPerfectNC_000002.11:g.132
017191_132089573du
p
GRCh37.p13First PassNC_000002.11Chr2132,017,191132,089,573

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)
nssv169192350.007436400
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