A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736526



Internal ID160192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40631760..40632698hg38UCSC Ensembl
chrX:40491012..40491950hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415868
Supporting Variants
Samples
Known GenesCXorf38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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