A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632579



Internal ID7019389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67964842..67980243hg38UCSC Ensembl
Innerchr13:67964842..67980243hg38UCSC Ensembl
Outerchr13:67964453..67980500hg38UCSC Ensembl
chr13:68538974..68554375hg19UCSC Ensembl
Innerchr13:68538974..68554375hg19UCSC Ensembl
Outerchr13:68538585..68554632hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3815402
hg1915402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782622, essv14782623
SamplesNA20905, HG02733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632579
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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