A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800812



Internal ID16094768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95617349..95618064hg38UCSC Ensembl
Innerchr12:96011125..96011840hg19UCSC Ensembl
Innerchr12:94535256..94535971hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38716
hg19716
hg18716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559822
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv800812
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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