A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594258



Internal ID21786301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31595356..31595469hg38UCSC Ensembl
chr10:31884284..31884397hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594258
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