A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740555



Internal ID164221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68807660..68807660hg38UCSC Ensembl
chrX:68027503..68027503hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740555
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007996


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