A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787842



Internal ID18822378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7582024..7893171hg38UCSC Ensembl
Innerchr20:7562671..7873818hg19UCSC Ensembl
Innerchr20:7510671..7821818hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38311148
hg19311148
hg18311148
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893279
Supporting Variants
Samples
Known GenesHAO1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787842
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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