A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443791



Internal ID22501661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135538143..135746481hg38UCSC Ensembl
chrX:134672068..134914912hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38208339
hg19242845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876021
Supporting Variants
Samples
Known GenesCT45A1, CT45A2, CT45A3, CT45A4, DDX26B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443791
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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