A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737906



Internal ID161572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149499000..149591606hg38UCSC Ensembl
chrX:148580531..148673270hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3892607
hg1992740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429574
Supporting Variants
Samples
Known GenesCXorf40A, IDS, LINC00893, MAGEA9, MAGEA9B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737906
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000209118


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