A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980219



Internal ID12634774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391871..31483699hg38UCSC Ensembl
Innerchr6:31359648..31451476hg19UCSC Ensembl
Innerchr6:31467627..31559455hg18UCSC Ensembl
Innerchr6:31467627..31559455hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3891829
hg1991829
hg1891829
hg1791829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34950
Supporting Variants
SamplesNA18969
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980219
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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