A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740954



Internal ID164620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79609275..79694130hg38UCSC Ensembl
chrX:78864772..78949627hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3884856
hg1984856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420551
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740954
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062435


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