A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983466



Internal ID12629659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167034693..167114544hg38UCSC Ensembl
Innerchr6:167448181..167528032hg19UCSC Ensembl
Innerchr6:167368171..167448022hg18UCSC Ensembl
Innerchr6:167418592..167498443hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3879852
hg1979852
hg1879852
hg1779852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752099
Supporting Variants
SamplesBEC_658
Known GenesCCR6, FGFR1OP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983466
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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