A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643881



Internal ID21835928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119808975..119824762hg38UCSC Ensembl
chrX:118942938..118958725hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3815788
hg1915788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643881
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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