A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893342



Internal ID19184162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47415238..47469940hg38UCSC Ensembl
Outerchr20:47415238..47469940hg38UCSC Ensembl
Innerchr20:46043982..46098684hg19UCSC Ensembl
Outerchr20:46043982..46098684hg19UCSC Ensembl
Innerchr20:45477389..45532091hg18UCSC Ensembl
Outerchr20:45477389..45532091hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3854703
hg1954703
hg1854703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783929
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893342
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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