A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14254805



Internal ID22131198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:126295149..126332042hg38UCSC Ensembl
Outerchr12:126779695..126816588hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3836894
hg1936894
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217008
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14254805
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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