A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740327



Internal ID163993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57985930..57986882hg38UCSC Ensembl
chrX:58012364..58013316hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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