A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519863



Internal ID18818144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55167766hg38UCSC Ensembl
Innerchr11:54720811..54935242hg19UCSC Ensembl
Innerchr11:54477387..54691818hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38214432
hg19214432
hg18214432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049068
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)nssv3519863
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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