A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633429



Internal ID7020238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104697657..104912897hg38UCSC Ensembl
Innerchr13:104697688..104912867hg38UCSC Ensembl
Outerchr13:104697627..104912928hg38UCSC Ensembl
chr13:105350008..105565248hg19UCSC Ensembl
Innerchr13:105350039..105565218hg19UCSC Ensembl
Outerchr13:105349978..105565279hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38215241
hg19215241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14886430
SamplesHG02561
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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