A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786709



Internal ID18836234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031284..54038172hg38UCSC Ensembl
Innerchr20:52647823..52654711hg19UCSC Ensembl
Innerchr20:52081230..52088118hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386889
hg196889
hg186889
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893347
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786709
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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