A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741842



Internal ID165508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106683464..106695369hg38UCSC Ensembl
chrX:105926694..105938599hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3811906
hg1911906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426334
Supporting Variants
Samples
Known GenesRNF128
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741842
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0012487


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