A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14895670



Internal ID4686902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109707186..109731351hg38UCSC Ensembl
chr13:110359533..110383698hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3824166
hg1924166
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633531
Supporting Variants
SamplesHG04210
Known GenesLINC00676
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14895670
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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