A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981894



Internal ID12974104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1678745..1834648hg38UCSC Ensembl
Innerchr18:1678746..1834649hg19UCSC Ensembl
Innerchr18:1668746..1824649hg18UCSC Ensembl
Innerchr18:1668746..1824649hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38155904
hg19155904
hg18155904
hg17155904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751772
Supporting Variants
SamplesBEC_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981894
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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