A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559465



Internal ID16346874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:81118979..81147286hg38UCSC Ensembl
Innerchr12:81512758..81541065hg19UCSC Ensembl
Innerchr12:80036889..80065196hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3828308
hg1928308
hg1828308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv798919
Samples
Known GenesACSS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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