A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138918



Internal ID338102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146801606..146823606hg38UCSC Ensembl
chrX:145883124..145905124hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737800
Samples
Known GenesCXorf51A, CXorf51B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138918
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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