A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012959



Internal ID18755490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168016004..168067497hg38UCSC Ensembl
Innerchr1:167985242..168036735hg19UCSC Ensembl
Innerchr1:166251866..166303359hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3851494
hg1951494
hg1851494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3497876, nssv3497080
Samples
Known GenesDCAF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012959
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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