A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798660



Internal ID19177040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:72456544..72466225hg38UCSC Ensembl
Innerchr13:73030682..73040363hg19UCSC Ensembl
Innerchr13:71928683..71938364hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389682
hg199682
hg189682
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892389
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798660
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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