A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893331



Internal ID19184151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36412885..36418818hg38UCSC Ensembl
Outerchr20:36412885..36418818hg38UCSC Ensembl
Innerchr20:35041288..35047221hg19UCSC Ensembl
Outerchr20:35041288..35047221hg19UCSC Ensembl
Innerchr20:34474702..34480635hg18UCSC Ensembl
Outerchr20:34474702..34480635hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385934
hg195934
hg185934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796749
Samples
Known GenesDLGAP4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893331
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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