A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15040397



Internal ID4105061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63589669..63596332hg38UCSC Ensembl
Innerchr14:63589724..63596277hg38UCSC Ensembl
Outerchr14:63589614..63596387hg38UCSC Ensembl
chr14:64056387..64063050hg19UCSC Ensembl
Innerchr14:64056442..64062995hg19UCSC Ensembl
Outerchr14:64056332..64063105hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg386664
hg196664
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634733
Supporting Variants
SamplesHG03729
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15040397
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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