A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742080



Internal ID165746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113984611..113989025hg38UCSC Ensembl
chrX:113227852..113232258hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384415
hg194407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742080
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002498


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