A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14839295



Internal ID3356809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89695872..89852183hg38UCSC Ensembl
chr13:90348126..90504437hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38156312
hg19156312
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633102
Supporting Variants
SamplesHG03009
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14839295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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