A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982362



Internal ID12973614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77749351..78083759hg38UCSC Ensembl
Innerchr8:78661586..78995994hg19UCSC Ensembl
Innerchr8:78824141..79158549hg18UCSC Ensembl
Innerchr8:78824141..79158549hg17UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38334409
hg19334409
hg18334409
hg17334409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752267
Supporting Variants
SamplesBEC_427
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982362
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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