A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621388



Internal ID21813435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26592326..26592385hg38UCSC Ensembl
chr16:26603647..26603706hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621388
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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