A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980090



Internal ID12634551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29903859..29931120hg38UCSC Ensembl
Innerchr6:29871636..29898897hg19UCSC Ensembl
Innerchr6:29979615..30006876hg18UCSC Ensembl
Innerchr6:29979615..30006876hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3827262
hg1927262
hg1827262
hg1727262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34987
Supporting Variants
SamplesNA18951
Known GenesHCG4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980090
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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