A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961168



Internal ID22736128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25042007..25042007hg38UCSC Ensembl
chrX:25060124..25060124hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961168
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