A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736091



Internal ID159757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3073530..3073530hg38UCSC Ensembl
chrX:2991571..2991571hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549102
Supporting Variants
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0389145


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