A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695886



Internal ID15432538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:65724729..65737283hg38UCSC Ensembl
Innerchr12:66118509..66131063hg19UCSC Ensembl
Innerchr12:64404776..64417330hg18UCSC Ensembl
Innerchr12:64404776..64417330hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3812555
hg1912555
hg1812555
hg1712555
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518448
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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