A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002349



Internal ID21911692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24657299..24657435hg38UCSC Ensembl
chr10:24946228..24946364hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578897
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002349
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