A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280117



Internal ID20489335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12261164..12261444hg38UCSC Ensembl
chr16:12355021..12355301hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734971
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280117
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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