A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15091374



Internal ID6018190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86785180..86913434hg38UCSC Ensembl
chr14:87251524..87379778hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38128255
hg19128255
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635238
Supporting Variants
SamplesNA19430
Known GenesLOC283585
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15091374
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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