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nsv4212936

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96,377

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 68 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):108,265,781-108,362,157Question Mark
Overlapping variant regions from other studies: 68 SVs from 14 studies. See in: genome view    
Submitted genomic108,659,558-108,755,934Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4212936RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12108,265,781108,362,157
nsv4212936Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr12108,659,558108,755,934

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15813408deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15813408RemappedPerfectNC_000012.12:g.108
265781_108362157de
l
GRCh38.p12First PassNC_000012.12Chr12108,265,781108,362,157
nssv15813408Submitted genomicNC_000012.11:g.108
659558_108755934de
l
GRCh37.p13NC_000012.11Chr12108,659,558108,755,934

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)
nssv158134084.6e-005121694
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