A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14881032



Internal ID6802218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103130054..103141603hg38UCSC Ensembl
chr13:103782404..103793953hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3811550
hg1911550
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633393
Supporting Variants
SamplesNA20890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14881032
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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