A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600866



Internal ID21792913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20820505..20820654hg38UCSC Ensembl
chr16:20831827..20831976hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027858
Supporting Variants
Samples
Known GenesLOC81691
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600866
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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