A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619932



Internal ID21811979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66789290..66789625hg38UCSC Ensembl
chr16:66823193..66823528hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027000
Supporting Variants
Samples
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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