A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288301



Internal ID20497519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:795413..795503hg38UCSC Ensembl
chr16:845413..845503hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735270
Supporting Variants
Samples
Known GenesCHTF18
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288301
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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