A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591198



Internal ID18889479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46806114hg38UCSC Ensembl
Innerchr3:46801805..46847604hg19UCSC Ensembl
Innerchr3:46776809..46822608hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3845800
hg1945800
hg1845800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000895
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)nssv3591198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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