A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012239



Internal ID18754775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46817977hg38UCSC Ensembl
Innerchr3:46801805..46859467hg19UCSC Ensembl
Innerchr3:46776809..46834471hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3857663
hg1957663
hg1857663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4732n100
Supporting Variantsnssv3593699, nssv3593703, nssv3593698, nssv3593701, nssv3593702, nssv3593700
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)nsv1012239
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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