A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15025904



Internal ID4072860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59397499..59401662hg38UCSC Ensembl
Innerchr14:59397543..59401618hg38UCSC Ensembl
Outerchr14:59397455..59401706hg38UCSC Ensembl
chr14:59864217..59868380hg19UCSC Ensembl
Innerchr14:59864261..59868336hg19UCSC Ensembl
Outerchr14:59864173..59868424hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg384164
hg194164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634647
Supporting Variants
SamplesHG03705
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15025904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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