A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632911



Internal ID7019722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83372014..83380428hg38UCSC Ensembl
Innerchr13:83372014..83380428hg38UCSC Ensembl
Outerchr13:83371514..83380928hg38UCSC Ensembl
chr13:83946149..83954563hg19UCSC Ensembl
Innerchr13:83946149..83954563hg19UCSC Ensembl
Outerchr13:83945649..83955063hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388415
hg198415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822134, essv14822132, essv14822133
SamplesHG00271, HG00154, HG00123
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632911
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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