A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739153



Internal ID162819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8280881..8427416hg38UCSC Ensembl
chrX:8248922..8395457hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38146536
hg19146536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000416233


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