A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6195n100



Internal ID22792282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167194096..167247175hg38UCSC Ensembl
chr6:167607584..167660663hg19UCSC Ensembl
chr6:167527574..167580653hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853080
hg1953080
hg1853080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029454, nsv1021664, nsv1028537, nsv1026183, nsv1021482, nsv1031416, nsv1033801
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6195n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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