A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035966



Internal ID18778497
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 StatusM
Merged Variantsdgv1212n100
Supporting Variantsnssv3517164, nssv3517311, nssv3510031
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)nsv1035966
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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