A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138042



Internal ID337224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146807606..146929606hg38UCSC Ensembl
chrX:145889124..146011124hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38122001
hg19122001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737801
Samples
Known GenesCXorf51A, CXorf51B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138042
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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