A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702446



Internal ID15439098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:65721421..65737283hg38UCSC Ensembl
Innerchr12:66115201..66131063hg19UCSC Ensembl
Innerchr12:64401468..64417330hg18UCSC Ensembl
Innerchr12:64401468..64417330hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3815863
hg1915863
hg1815863
hg1715863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526184
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702446
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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