A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985800



Internal ID12984050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136873905hg38UCSC Ensembl
Innerchr8:137687955..137886148hg19UCSC Ensembl
Innerchr8:137757137..137955330hg18UCSC Ensembl
Innerchr8:137757137..137955330hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38198194
hg19198194
hg18198194
hg17198194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35104
Supporting Variants
SamplesSPC_52
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985800
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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