A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980600



Internal ID21889943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110930071..110935092hg38UCSC Ensembl
chr1:111472693..111477714hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980600
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