A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740489



Internal ID164155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67450542..67474542hg38UCSC Ensembl
chrX:66670384..66694384hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3824001
hg1924001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000419111


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