A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737908



Internal ID161574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149533600..149549606hg38UCSC Ensembl
chrX:148615135..148631151hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3816007
hg1916017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426950
Supporting Variants
Samples
Known GenesCXorf40A, LINC00893
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737908
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000210926


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