A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787663



Internal ID19174292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61718613..61740822hg38UCSC Ensembl
Innerchr20:60293669..60315878hg19UCSC Ensembl
Innerchr20:59727064..59749273hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3822210
hg1922210
hg1822210
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893356
Supporting Variants
Samples
Known GenesCDH4
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787663
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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