A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14985706



Internal ID6000037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41261847..41340957hg38UCSC Ensembl
chr14:41731050..41810160hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3879111
hg1979111
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634199
Supporting Variants
SamplesNA19399
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14985706
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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