A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739441



Internal ID163107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16647974..16674660hg38UCSC Ensembl
chrX:16666097..16692783hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3826687
hg1926687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139011
Supporting Variants
Samples
Known GenesCTPS2, S100G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00166493


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