A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963369



Internal ID15910639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58472009..58557785hg38UCSC Ensembl
Innerchr3:58457736..58543512hg19UCSC Ensembl
Innerchr3:58432776..58518552hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3885777
hg1985777
hg1885777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590370
Supporting Variants
Samples
Known GenesACOX2, KCTD6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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