A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138059



Internal ID337241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135658227..135735474hg38UCSC Ensembl
chrX:134791942..134903901hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3877248
hg19111960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv579n206
Supporting Variantsnssv17742492
Samples
Known GenesCT45A1, CT45A2, CT45A3, CT45A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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