A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046559



Internal ID18789090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60991561..61103348hg38UCSC Ensembl
Innerchr11:60759033..60870820hg19UCSC Ensembl
Innerchr11:60515609..60627396hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38111788
hg19111788
hg18111788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1212n100
Supporting Variantsnssv3513077
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)nsv1046559
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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