A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6197n100



Internal ID19016565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167267069..167382413hg38UCSC Ensembl
chr6:167680557..167795901hg19UCSC Ensembl
chr6:167600547..167715891hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38115345
hg19115345
hg18115345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026070, nsv1027513, nsv1030424, nsv1028156, nsv1031235, nsv1017981
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)dgv6197n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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