A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138455



Internal ID337639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153075141..153086553hg38UCSC Ensembl
chrX:152243524..152352406hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811413
hg19108883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738051
Samples
Known GenesPNMA6A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138455
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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