A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892325



Internal ID19183145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33364004..33704782hg38UCSC Ensembl
Outerchr13:33364004..33704782hg38UCSC Ensembl
Innerchr13:33938141..34278919hg19UCSC Ensembl
Outerchr13:33938141..34278919hg19UCSC Ensembl
Innerchr13:32836141..33176919hg18UCSC Ensembl
Outerchr13:32836141..33176919hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38340779
hg19340779
hg18340779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778966
Samples
Known GenesSTARD13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892325
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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