A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6194n100



Internal ID19016562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167156031..167425505hg38UCSC Ensembl
chr6:167569519..167838993hg19UCSC Ensembl
chr6:167489509..167758983hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38269475
hg19269475
hg18269475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019368, nsv1032268
Samples
Known GenesGPR31, TCP10, TCP10L2, 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)dgv6194n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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