A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632590



Internal ID7019400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68302655..68303374hg38UCSC Ensembl
Innerchr13:68302655..68303374hg38UCSC Ensembl
Outerchr13:68302493..68303521hg38UCSC Ensembl
chr13:68876787..68877506hg19UCSC Ensembl
Innerchr13:68876787..68877506hg19UCSC Ensembl
Outerchr13:68876625..68877653hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782681
SamplesHG01171
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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