A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979502



Internal ID12980281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31265733..31309909hg38UCSC Ensembl
Innerchr6:31233510..31277686hg19UCSC Ensembl
Innerchr6:31341489..31385665hg18UCSC Ensembl
Innerchr6:31341489..31385665hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3844177
hg1944177
hg1844177
hg1744177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35158
Supporting Variants
SamplesNA18563
Known GenesHLA-C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979502
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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