A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922981



Internal ID16076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206134512..206135530hg38UCSC Ensembl
chr2:206999236..207000254hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434300
Supporting Variants
Samples
Known GenesNDUFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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