A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608240



Internal ID21800287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60421360..60422764hg38UCSC Ensembl
chr15:60713559..60714963hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032652
Supporting Variants
Samples
Known GenesNARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608240
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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