A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789509



Internal ID19169438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23697192..23752605hg38UCSC Ensembl
Innerchr20:23677829..23733242hg19UCSC Ensembl
Innerchr20:23625829..23681242hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3855414
hg1955414
hg1855414
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893321
Supporting Variants
Samples
Known GenesCST1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789509
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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