A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266031



Internal ID20475249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32762463..32762463hg38UCSC Ensembl
chr5:32762569..32762569hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766025
Supporting Variants
Samples
Known GenesNPR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266031
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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