A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633473



Internal ID6673595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106857673..106865812hg38UCSC Ensembl
Innerchr13:106857673..106865812hg38UCSC Ensembl
Outerchr13:106857429..106866086hg38UCSC Ensembl
chr13:107510021..107518160hg19UCSC Ensembl
Innerchr13:107510021..107518160hg19UCSC Ensembl
Outerchr13:107509777..107518434hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg388140
hg198140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14890387, essv14890388
SamplesHG01070, HG00732
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633473
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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