A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785829



Internal ID19163068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25805665..25970656hg38UCSC Ensembl
Innerchr20:25786301..25951292hg19UCSC Ensembl
Innerchr20:25734301..25899292hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38164992
hg19164992
hg18164992
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893325
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785829
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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