A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778256



Internal ID18833460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14707873..14884242hg38UCSC Ensembl
Innerchr20:14688519..14864888hg19UCSC Ensembl
Innerchr20:14636519..14812888hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38176370
hg19176370
hg18176370
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893296
Supporting Variants
Samples
Known GenesMACROD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778256
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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