A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488019



Internal ID21145572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69055401..69058000hg38UCSC Ensembl
chr14:69522118..69524717hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020581
Samples
Known GenesDCAF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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