A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633038



Internal ID7019848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87291663..87311537hg38UCSC Ensembl
Innerchr13:87291681..87311519hg38UCSC Ensembl
Outerchr13:87291645..87311555hg38UCSC Ensembl
chr13:87943918..87963792hg19UCSC Ensembl
Innerchr13:87943936..87963774hg19UCSC Ensembl
Outerchr13:87943900..87963810hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3819875
hg1919875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14834657, essv14834656
SamplesHG03225, HG03073
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633038
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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