A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15092065



Internal ID6182159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87239670..87246149hg38UCSC Ensembl
Innerchr14:87239670..87246149hg38UCSC Ensembl
Outerchr14:87239584..87246214hg38UCSC Ensembl
chr14:87706014..87712493hg19UCSC Ensembl
Innerchr14:87706014..87712493hg19UCSC Ensembl
Outerchr14:87705928..87712558hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386480
hg196480
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635255
Supporting Variants
SamplesNA19717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15092065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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