A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037372



Internal ID92665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67902278..67903622hg38UCSC Ensembl
chr10:69662036..69663380hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486513
Supporting Variants
Samples
Known GenesSIRT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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