A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779786



Internal ID18825518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51984900..52012065hg38UCSC Ensembl
Innerchr20:50601439..50628604hg19UCSC Ensembl
Innerchr20:50034846..50062011hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3827166
hg1927166
hg1827166
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893346
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779786
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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