A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740173



Internal ID163839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54854800..54860964hg38UCSC Ensembl
chrX:54881233..54887397hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg386165
hg196165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740173
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125444


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