A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794359



Internal ID21239697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59078582..59078888hg38UCSC Ensembl
chr14:59545300..59545606hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794359
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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