A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632899



Internal ID7019710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82940895..83050025hg38UCSC Ensembl
Innerchr13:82941045..83049875hg38UCSC Ensembl
Outerchr13:82940745..83050175hg38UCSC Ensembl
chr13:83515030..83624160hg19UCSC Ensembl
Innerchr13:83515180..83624010hg19UCSC Ensembl
Outerchr13:83514880..83624310hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38109131
hg19109131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv355e214
Supporting Variantsessv14821620
SamplesHG03944
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632899
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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