A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024496



Internal ID21933839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62885553..62942587hg38UCSC Ensembl
chr14:63352271..63409305hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3857035
hg1957035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609958
Samples
Known GenesKCNH5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024496
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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