A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781768



Internal ID19179489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61178256..61184733hg38UCSC Ensembl
Innerchr20:59753312..59759789hg19UCSC Ensembl
Innerchr20:59186707..59193184hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386478
hg196478
hg186478
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893355
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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