A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799584



Internal ID19160254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16285977..16291544hg38UCSC Ensembl
Innerchr20:16266622..16272189hg19UCSC Ensembl
Innerchr20:16214622..16220189hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg385568
hg195568
hg185568
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893318
Supporting Variants
Samples
Known GenesKIF16B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799584
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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