A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738141



Internal ID161807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154646606..154653803hg38UCSC Ensembl
chrX:153874880..153882077hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387198
hg197198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138196
Supporting Variants
Samples
Known GenesCTAG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738141
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000862317


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