A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706781



Internal ID130447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2515655..2515722hg38UCSC Ensembl
chr16:2565656..2565723hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532266
Supporting Variants
Samples
Known GenesATP6V0C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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