A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020942



Internal ID21930285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60242576..60243168hg38UCSC Ensembl
chr14:60709294..60709886hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020942
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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