A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797690



Internal ID19178803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61179529..61187161hg38UCSC Ensembl
Innerchr20:59754585..59762217hg19UCSC Ensembl
Innerchr20:59187980..59195612hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387633
hg197633
hg187633
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893355
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797690
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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