A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139110



Internal ID338294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154495410..154525459hg38UCSC Ensembl
chrX:153723760..153753677hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3830050
hg1929918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738119
Samples
Known GenesFAM3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139110
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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