A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741861



Internal ID165527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107418230..107418230hg38UCSC Ensembl
chrX:106661460..106661460hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741861
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.32542


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