A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14888864



Internal ID6271783
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633448
Supporting Variants
SamplesNA19789
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14888864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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