A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519203



Internal ID18817484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85153507..85209276hg38UCSC Ensembl
Innerchr11:84864551..84920320hg19UCSC Ensembl
Innerchr11:84542199..84597968hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3855770
hg1955770
hg1855770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052380
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519203
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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