A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027767



Internal ID21937110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103918430..103918534hg38UCSC Ensembl
chr14:104384767..104384871hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606614
Samples
Known GenesC14orf2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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