A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520186



Internal ID18818467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80274228hg38UCSC Ensembl
Innerchr11:79967536..79985272hg19UCSC Ensembl
Innerchr11:79645184..79662920hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817737
hg1917737
hg1817737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053741
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)nssv3520186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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