A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736782



Internal ID160448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47258203..47294721hg38UCSC Ensembl
chrX:47117602..47154120hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3836519
hg1936519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000208117


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