A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034858



Internal ID21944201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67686522..67686585hg38UCSC Ensembl
chr14:68153239..68153302hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598392
Samples
Known GenesRDH11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034858
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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