A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14937160



Internal ID874438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23728697..23739592hg38UCSC Ensembl
Innerchr14:23728703..23739586hg38UCSC Ensembl
Outerchr14:23728691..23739598hg38UCSC Ensembl
chr14:24197906..24208801hg19UCSC Ensembl
Innerchr14:24197912..24208795hg19UCSC Ensembl
Outerchr14:24197900..24208807hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3810896
hg1910896
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633782
Supporting Variants
SamplesHG00464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14937160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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