A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736106



Internal ID159772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3339488..3629488hg38UCSC Ensembl
chrX:3257529..3547529hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38290001
hg19290001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137945
Supporting Variants
Samples
Known GenesMXRA5, PRKX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000835596


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