A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628129



Internal ID21820176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67479904..67480221hg38UCSC Ensembl
chr16:67513807..67514124hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025499
Supporting Variants
Samples
Known GenesATP6V0D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628129
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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