A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632878



Internal ID7019689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81952185..82016541hg38UCSC Ensembl
chr13:82526320..82590676hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3864357
hg1964357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv354e214
Supporting Variantsessv14820064, essv14820069, essv14820066, essv14820070, essv14820067, essv14820065, essv14820068
SamplesHG03926, HG04214, HG03780, HG03781, NA21102, NA21093, HG03864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632878
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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