A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632766



Internal ID7019577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76197593..76201425hg38UCSC Ensembl
Innerchr13:76197593..76201425hg38UCSC Ensembl
Outerchr13:76197093..76201925hg38UCSC Ensembl
chr13:76771729..76775561hg19UCSC Ensembl
Innerchr13:76771729..76775561hg19UCSC Ensembl
Outerchr13:76771229..76776061hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14800924, essv14800925
SamplesHG02017, HG02450
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632766
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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