A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597273



Internal ID21789316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24710937..24710937hg38UCSC Ensembl
chr10:24999866..24999866hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089514
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597273
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