nsv5542712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,966

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 29 studies. See in: genome view    
Submitted genomic34,061,196-34,067,161Question Mark
Overlapping variant regions from other studies: 105 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):34,457,185-34,463,150Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5542712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2234,061,19634,067,161
nsv5542712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2234,457,18534,463,150

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728634deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728634Submitted genomicNC_000022.11:g.340
61196_34067161del
GRCh38 (hg38)NC_000022.11Chr2234,061,19634,067,161
nssv17728634RemappedPerfectNC_000022.10:g.344
57185_34463150del
GRCh37.p13First PassNC_000022.10Chr2234,457,18534,463,150

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)
nssv17728634<0.00126404
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