A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513301



Internal ID18464896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76158391..76197866hg38UCSC Ensembl
Innerchr11:75869435..75908910hg19UCSC Ensembl
Innerchr11:75547083..75586558hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3839476
hg1939476
hg1839476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041667
Supporting Variants
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513301
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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