A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708662



Internal ID132328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77724236..77724238hg38UCSC Ensembl
chr16:77758133..77758135hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544949
Supporting Variants
Samples
Known GenesNUDT7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708662
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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