A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646200



Internal ID21838247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155967078..155981305hg38UCSC Ensembl
chrX:155196743..155210970hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814228
hg1914228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108762
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646200
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