A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979741



Internal ID12633987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31394533..31489801hg38UCSC Ensembl
Innerchr6:31362310..31457578hg19UCSC Ensembl
Innerchr6:31470289..31565557hg18UCSC Ensembl
Innerchr6:31470289..31565557hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3895269
hg1995269
hg1895269
hg1795269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34991
Supporting Variants
SamplesNA18620
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979741
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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