A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978141



Internal ID12981494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90138498..90198244hg38UCSC Ensembl
Innerchr8:91150726..91210472hg19UCSC Ensembl
Innerchr8:91219902..91279648hg18UCSC Ensembl
Innerchr8:91219902..91279648hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3859747
hg1959747
hg1859747
hg1759747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35109
Supporting Variants
SamplesNA18971
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978141
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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