A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15039033



Internal ID6176453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63192302..63193426hg38UCSC Ensembl
Innerchr14:63192352..63193376hg38UCSC Ensembl
Outerchr14:63192252..63193476hg38UCSC Ensembl
chr14:63659020..63660144hg19UCSC Ensembl
Innerchr14:63659070..63660094hg19UCSC Ensembl
Outerchr14:63658970..63660194hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634721
Supporting Variants
SamplesNA19713
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15039033
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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