A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742099



Internal ID165765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114395198..114411198hg38UCSC Ensembl
chrX:113629651..113645651hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292948


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