A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469065



Internal ID22526956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47549247..47559115hg38UCSC Ensembl
chrX:47408646..47418514hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg389869
hg199869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469065
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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