A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736479



Internal ID160145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39782181..39805273hg38UCSC Ensembl
chrX:39641435..39664527hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3823093
hg1923093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736479
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00166493


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