A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979680



Internal ID53830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13524856..13607768hg38UCSC Ensembl
chr6:13525088..13608000hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3882913
hg1982913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466612
Supporting Variants
Samples
Known GenesSIRT5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979680
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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