A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742098



Internal ID165764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114366090..114367456hg38UCSC Ensembl
chrX:113600543..113601909hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742098
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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