A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402755



Internal ID22460625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86359213..86361883hg38UCSC Ensembl
chr2:86586336..86589006hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382671
hg192671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer