A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741447



Internal ID165113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92100004..92100063hg38UCSC Ensembl
chrX:91355003..91355062hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421940
Supporting Variants
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741447
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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