A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742596



Internal ID166262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138021431..138022535hg38UCSC Ensembl
chrX:137103590..137104694hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420654
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742596
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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