A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601971



Internal ID21794018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4149357..4160177hg38UCSC Ensembl
chr16:4199358..4210178hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810821
hg1910821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601971
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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