A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520681



Internal ID18818962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80274585hg38UCSC Ensembl
Innerchr11:79967536..79985629hg19UCSC Ensembl
Innerchr11:79645184..79663277hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3818094
hg1918094
hg1818094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052871
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)nssv3520681
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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