A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606031



Internal ID21798078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3129152..3132323hg38UCSC Ensembl
chr16:3179153..3182324hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383172
hg193172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606031
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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