A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138079



Internal ID337261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152869384..153060570hg38UCSC Ensembl
chrX:152037928..152228930hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38191187
hg19191003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738038
Samples
Known GenesPNMA3, PNMA5, ZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138079
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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