A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589536



Internal ID18887817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26129208..26155808hg38UCSC Ensembl
Innerchr3:26170699..26197299hg19UCSC Ensembl
Innerchr3:26145703..26172303hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3826601
hg1926601
hg1826601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013837
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)nssv3589536
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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