A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14967711



Internal ID5798576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35426870..35429253hg38UCSC Ensembl
Innerchr14:35426893..35429230hg38UCSC Ensembl
Outerchr14:35426847..35429276hg38UCSC Ensembl
chr14:35896076..35898459hg19UCSC Ensembl
Innerchr14:35896099..35898436hg19UCSC Ensembl
Outerchr14:35896053..35898482hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382384
hg192384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634060
Supporting Variants
SamplesNA19171
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14967711
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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