A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796103



Internal ID18813110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9260191..9278724hg38UCSC Ensembl
Innerchr20:9240838..9259371hg19UCSC Ensembl
Innerchr20:9188838..9207371hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3818534
hg1918534
hg1818534
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893285
Supporting Variants
Samples
Known GenesPLCB4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796103
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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