A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14886435



Internal ID6723660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104987919..105045434hg38UCSC Ensembl
chr13:105640270..105697785hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3857516
hg1957516
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633434
Supporting Variants
SamplesNA20852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14886435
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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