A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960275



Internal ID22735260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57329219..57329816hg38UCSC Ensembl
chr20:55904275..55904872hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393473
Samples
Known GenesSPO11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960275
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