A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14895718



Internal ID5576134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109808679..109816882hg38UCSC Ensembl
Innerchr13:109808692..109816870hg38UCSC Ensembl
Outerchr13:109808667..109816895hg38UCSC Ensembl
chr13:110461026..110469229hg19UCSC Ensembl
Innerchr13:110461039..110469217hg19UCSC Ensembl
Outerchr13:110461014..110469242hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg388204
hg198204
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633535
Supporting Variants
SamplesNA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14895718
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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