A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138023



Internal ID337205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:266351..281000hg38UCSC Ensembl
chrX:183018..197667hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3814650
hg1914650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735947
Samples
Known GenesPLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138023
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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