A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14895671



Internal ID4686851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109707303..109733040hg38UCSC Ensembl
Innerchr13:109707313..109733031hg38UCSC Ensembl
Outerchr13:109707294..109733050hg38UCSC Ensembl
chr13:110359650..110385387hg19UCSC Ensembl
Innerchr13:110359660..110385378hg19UCSC Ensembl
Outerchr13:110359641..110385397hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3825738
hg1925738
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633532
Supporting Variants
SamplesHG04210
Known GenesLINC00676
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14895671
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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