A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882562



Internal ID22657539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67385070..67386147hg38UCSC Ensembl
chr2:67612202..67613279hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882562
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