A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14946889



Internal ID6860363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26625031..26683599hg38UCSC Ensembl
chr14:27094237..27152805hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3858569
hg1958569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633853
Supporting Variants
SamplesNA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14946889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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