A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881576



Internal ID22656552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31743142..31898199hg38UCSC Ensembl
chr2:31968211..32123268hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38155058
hg19155058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399462
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881576
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