A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982061



Internal ID12627677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391844..31488044hg38UCSC Ensembl
Innerchr6:31359621..31455821hg19UCSC Ensembl
Innerchr6:31467600..31563800hg18UCSC Ensembl
Innerchr6:31467600..31563800hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896201
hg1996201
hg1896201
hg1796201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752119
Supporting Variants
SamplesBEC_516
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982061
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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