A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632920



Internal ID7019731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83602220..83687881hg38UCSC Ensembl
Innerchr13:83602241..83687861hg38UCSC Ensembl
Outerchr13:83602200..83687902hg38UCSC Ensembl
chr13:84176355..84262016hg19UCSC Ensembl
Innerchr13:84176376..84261996hg19UCSC Ensembl
Outerchr13:84176335..84262037hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3885662
hg1985662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822349
SamplesNA18561
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632920
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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