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nsv4289064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,806

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):35,064,783-35,171,588Question Mark
Overlapping variant regions from other studies: 96 SVs from 16 studies. See in: genome view    
Submitted genomic35,460,776-35,567,581Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4289064RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2235,064,78335,171,588
nsv4289064Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2235,460,77635,567,581

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15862841deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15862841RemappedPerfectNC_000022.11:g.350
64783_35171588del
GRCh38.p12First PassNC_000022.11Chr2235,064,78335,171,588
nssv15862841Submitted genomicNC_000022.10:g.354
60776_35567581del
GRCh37.p13NC_000022.10Chr2235,460,77635,567,581

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)
nssv158628414.6e-005121694
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