A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282513



Internal ID20491731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46016091..46016162hg38UCSC Ensembl
chr6:45983828..45983899hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740617
Supporting Variants
Samples
Known GenesCLIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282513
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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