A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526032



Internal ID21850390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60575829..60575829hg38UCSC Ensembl
chr2:60802964..60802964hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526032
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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