A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893285



Internal ID18837419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9260191..9278724hg38UCSC Ensembl
Outerchr20:9260191..9278724hg38UCSC Ensembl
Innerchr20:9240838..9259371hg19UCSC Ensembl
Outerchr20:9240838..9259371hg19UCSC Ensembl
Innerchr20:9188838..9207371hg18UCSC Ensembl
Outerchr20:9188838..9207371hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3818534
hg1918534
hg1818534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796103
Samples
Known GenesPLCB4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893285
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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