A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601327



Internal ID21793374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60444105..60444105hg38UCSC Ensembl
chr15:60736304..60736304hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099619
Supporting Variants
Samples
Known GenesNARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601327
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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