A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629277



Internal ID21821324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50579497..50579610hg38UCSC Ensembl
chr16:50613408..50613521hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034323
Supporting Variants
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629277
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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