A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876021



Internal ID22650981
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 StatusM
Merged Variants
Supporting Variantsnssv17443791
Samples
Known GenesCT45A1, CT45A2, CT45A3, CT45A4, DDX26B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876021
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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