A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789867



Internal ID16083823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25119093..25188243hg38UCSC Ensembl
Innerchr12:25272027..25341177hg19UCSC Ensembl
Innerchr12:25163294..25232444hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3869151
hg1969151
hg1869151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557797
Supporting Variants
Samples
Known GenesCASC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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