A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290160



Internal ID20499378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85963330..85963951hg38UCSC Ensembl
chr16:85996936..85997557hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290160
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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