A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603394



Internal ID21795441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20908106..20914128hg38UCSC Ensembl
chr16:20919428..20925450hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg386023
hg196023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031286
Supporting Variants
Samples
Known GenesLYRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603394
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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