A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593159



Internal ID18891440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21840844..21864139hg38UCSC Ensembl
Innerchr3:21882336..21905631hg19UCSC Ensembl
Innerchr3:21857340..21880635hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823296
hg1923296
hg1823296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005321
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593159
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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