A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580077



Internal ID21772120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91364142..91366100hg38UCSC Ensembl
chr10:93123899..93125857hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381959
hg191959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009817
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580077
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