A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631099



Internal ID21823146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74613051..74613169hg38UCSC Ensembl
chr16:74646949..74647067hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631099
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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