A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634627



Internal ID7021430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58578362..58589975hg38UCSC Ensembl
Innerchr14:58578394..58589944hg38UCSC Ensembl
Outerchr14:58578331..58590007hg38UCSC Ensembl
chr14:59045080..59056693hg19UCSC Ensembl
Innerchr14:59045112..59056662hg19UCSC Ensembl
Outerchr14:59045049..59056725hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3811614
hg1911614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15024920, essv15024921
SamplesHG01097, HG01191
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634627
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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