A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982528



Internal ID12628448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8251046..8302222hg38UCSC Ensembl
Innerchr8:8108568..8159744hg19UCSC Ensembl
Innerchr8:8145978..8197154hg18UCSC Ensembl
Innerchr8:8145978..8197154hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3851177
hg1951177
hg1851177
hg1751177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752266
Supporting Variants
SamplesBEC_563
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982528
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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