A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736915



Internal ID160581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50092650..50092725hg38UCSC Ensembl
chrX:49857307..49857382hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421058
Supporting Variants
Samples
Known GenesCLCN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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