A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983578



Internal ID12976520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675575..136813575hg38UCSC Ensembl
Innerchr8:137687818..137825818hg19UCSC Ensembl
Innerchr8:137757000..137895000hg18UCSC Ensembl
Innerchr8:137757000..137895000hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38138001
hg19138001
hg18138001
hg17138001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35111
Supporting Variants
SamplesBEC_669
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983578
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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