A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591638



Internal ID21783681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71226294..71227185hg38UCSC Ensembl
chr10:72986051..72986942hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014400
Supporting Variants
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591638
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