A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431893



Internal ID210655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95018582..95020557hg38UCSC Ensembl
chrX:94273581..94275556hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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