A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509471



Internal ID18807752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67928175hg38UCSC Ensembl
Innerchr11:67501626..67695646hg19UCSC Ensembl
Innerchr11:67258202..67452222hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38194021
hg19194021
hg18194021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039721
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509471
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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