A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958925



Internal ID22719097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22663390..22663390hg38UCSC Ensembl
chr6:22663619..22663619hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958925
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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