A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638632



Internal ID21830679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:820029..1341297hg38UCSC Ensembl
chrX:780764..1460190hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38521269
hg19679427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109263
Supporting Variants
Samples
Known GenesCRLF2, CSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638632
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