A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636772



Internal ID21828819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68457281..68458088hg38UCSC Ensembl
chr16:68491184..68491991hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636772
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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