A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742514



Internal ID166180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135951378..135957960hg38UCSC Ensembl
chrX:135033537..135040119hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386583
hg196583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00228928


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