A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634828



Internal ID7021628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68630069..68630710hg38UCSC Ensembl
Innerchr14:68630105..68630675hg38UCSC Ensembl
Outerchr14:68630034..68630746hg38UCSC Ensembl
chr14:69096786..69097427hg19UCSC Ensembl
Innerchr14:69096822..69097392hg19UCSC Ensembl
Outerchr14:69096751..69097463hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15051195
SamplesHG01915
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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