A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741584



Internal ID165250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95539122..95540015hg38UCSC Ensembl
chrX:94794121..94795014hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741584
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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