A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740909



Internal ID20516886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100972301..100972301hg38UCSC Ensembl
chrX:100227290..100227290hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278884
Samples
Known GenesARL13A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740909
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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