A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742261



Internal ID165927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125967261..126156575hg38UCSC Ensembl
chrX:125101243..125290558hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38189315
hg19189316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742261
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00457856


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