A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532187



Internal ID21856543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24513161..24513582hg38UCSC Ensembl
chr1:24839651..24840072hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983171
Supporting Variants
Samples
Known GenesRCAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532187
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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