A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640983



Internal ID21833030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2449582..2483215hg38UCSC Ensembl
chrX:2367623..2401256hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3833634
hg1933634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111517
Supporting Variants
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640983
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