A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618393



Internal ID21810440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88442382..88449817hg38UCSC Ensembl
chr16:88508790..88516225hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg387436
hg197436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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