A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737321



Internal ID160987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119334758..119371581hg38UCSC Ensembl
chrX:118468721..118505544hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3836824
hg1936824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737321
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00104058


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