A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960206



Internal ID22735207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22346954..22346954hg38UCSC Ensembl
chrX:22365071..22365071hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462654
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960206
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