A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038051



Internal ID21947394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67136543..67136652hg38UCSC Ensembl
chr16:67170446..67170555hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625911
Samples
Known GenesC16orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038051
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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