A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522063



Internal ID18820344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15159377..15175514hg38UCSC Ensembl
Innerchr11:15180923..15197060hg19UCSC Ensembl
Innerchr11:15137499..15153636hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3816138
hg1916138
hg1816138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053222
Supporting Variants
Samples
Known GenesINSC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522063
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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