A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520436



Internal ID18818717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80270531hg38UCSC Ensembl
Innerchr11:79967536..79981575hg19UCSC Ensembl
Innerchr11:79645184..79659223hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814040
hg1914040
hg1814040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055057
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)nssv3520436
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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