A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739402



Internal ID163068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15504398..15558769hg38UCSC Ensembl
chrX:15522521..15576892hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3854372
hg1954372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428757
Supporting Variants
Samples
Known GenesBMX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739402
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000208117


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