A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633448



Internal ID7020257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105574479..105655588hg38UCSC Ensembl
Innerchr13:105574495..105655573hg38UCSC Ensembl
Outerchr13:105574464..105655604hg38UCSC Ensembl
chr13:106226828..106307937hg19UCSC Ensembl
Innerchr13:106226844..106307922hg19UCSC Ensembl
Outerchr13:106226813..106307953hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3881110
hg1981110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv366e214
Supporting Variantsessv14888864, essv14888862, essv14888863
SamplesNA19789, HG01149, NA19783
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633448
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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