A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6196n100



Internal ID19016564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167194096..167396465hg38UCSC Ensembl
chr6:167607584..167809953hg19UCSC Ensembl
chr6:167527574..167729943hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38202370
hg19202370
hg18202370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017088, nsv1024830, nsv1031882
Samples
Known GenesTCP10, TTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6196n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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