A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989809



Internal ID12976457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1897929..1980259hg38UCSC Ensembl
Innerchr18:1897930..1980260hg19UCSC Ensembl
Innerchr18:1887930..1970260hg18UCSC Ensembl
Innerchr18:1887930..1970260hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3882331
hg1982331
hg1882331
hg1782331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751775
Supporting Variants
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989809
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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