A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736240



Internal ID159906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26217620..26218289hg38UCSC Ensembl
chrX:26235737..26236406hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429537
Supporting Variants
Samples
Known GenesMAGEB5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736240
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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