A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261770



Internal ID20470988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2282711..2282782hg38UCSC Ensembl
chr16:2332712..2332783hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737051
Supporting Variants
Samples
Known GenesABCA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261770
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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