A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517164



Internal ID18468759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60991561..61113194hg38UCSC Ensembl
Innerchr11:60759033..60880666hg19UCSC Ensembl
Innerchr11:60515609..60637242hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38121634
hg19121634
hg18121634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035966
Supporting Variants
Samples
Known GenesCD5, CD6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517164
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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