A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632155



Internal ID7018965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55324474..55468206hg38UCSC Ensembl
Innerchr13:55324505..55468175hg38UCSC Ensembl
Outerchr13:55324443..55468237hg38UCSC Ensembl
chr13:55898609..56042341hg19UCSC Ensembl
Innerchr13:55898640..56042310hg19UCSC Ensembl
Outerchr13:55898578..56042372hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38143733
hg19143733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14735071
SamplesNA19085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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