A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14964789



Internal ID6957358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34077454..34087949hg38UCSC Ensembl
chr14:34546660..34557155hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3810496
hg1910496
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634020
Supporting Variants
SamplesNA21135
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14964789
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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