A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979148



Internal ID53478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14731450..14731549hg38UCSC Ensembl
chr6:14731681..14731780hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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