A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979073



Internal ID12979576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136850192hg38UCSC Ensembl
Innerchr8:137687955..137862435hg19UCSC Ensembl
Innerchr8:137757137..137931617hg18UCSC Ensembl
Innerchr8:137757137..137931617hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38174481
hg19174481
hg18174481
hg17174481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34324
Supporting Variants
SamplesNA12874
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979073
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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