A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893346



Internal ID18837480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51984900..52012065hg38UCSC Ensembl
Outerchr20:51984900..52012065hg38UCSC Ensembl
Innerchr20:50601439..50628604hg19UCSC Ensembl
Outerchr20:50601439..50628604hg19UCSC Ensembl
Innerchr20:50034846..50062011hg18UCSC Ensembl
Outerchr20:50034846..50062011hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3827166
hg1927166
hg1827166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779786
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893346
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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