A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1212n100



Internal ID19011580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60991561..61113994hg38UCSC Ensembl
chr11:60759033..60881466hg19UCSC Ensembl
chr11:60515609..60638042hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38122434
hg19122434
hg18122434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040188, nsv1035966, nsv1042804, nsv1046559
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)dgv1212n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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