A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276544



Internal ID20485762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58933887..58941360hg38UCSC Ensembl
chr16:58967791..58975264hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387474
hg197474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276544
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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