A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033952



Internal ID21943295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96049504..96049613hg38UCSC Ensembl
chr14:96515841..96515950hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605382
Samples
Known GenesC14orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033952
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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