A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532481



Internal ID21856837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9142013..9142013hg38UCSC Ensembl
chr2:9282142..9282142hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040652
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532481
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer