A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988178



Internal ID12633508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391871..31489801hg38UCSC Ensembl
Innerchr6:31359648..31457578hg19UCSC Ensembl
Innerchr6:31467627..31565557hg18UCSC Ensembl
Innerchr6:31467627..31565557hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897931
hg1997931
hg1897931
hg1797931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34444
Supporting Variants
SamplesNA18558
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988178
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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