A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432120



Internal ID210875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135538190..135671381hg38UCSC Ensembl
chrX:134672115..134805096hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38133192
hg19132982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742479
Samples
Known GenesDDX26B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432120
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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