A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv794065



Internal ID16088021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:42623723..42629144hg38UCSC Ensembl
Innerchr12:43017525..43022946hg19UCSC Ensembl
Innerchr12:41303792..41309213hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg385422
hg195422
hg185422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558705
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)nssv794065
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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