A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740504



Internal ID164170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67888053..67899775hg38UCSC Ensembl
chrX:67107895..67119617hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3811723
hg1911723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740504
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625391


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