A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983467



Internal ID12629660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167034693..167165614hg38UCSC Ensembl
Innerchr6:167448181..167579102hg19UCSC Ensembl
Innerchr6:167368171..167499092hg18UCSC Ensembl
Innerchr6:167418592..167549513hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38130922
hg19130922
hg18130922
hg17130922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752099
Supporting Variants
SamplesBEC_658
Known GenesCCR6, FGFR1OP, GPR31
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983467
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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