A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741965



Internal ID165631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110695374..110698911hg38UCSC Ensembl
chrX:109938602..109942139hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383538
hg193538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431269
Supporting Variants
Samples
Known GenesCHRDL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005776


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