A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422026



Internal ID201082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65129475..65134914hg38UCSC Ensembl
chrX:64349355..64354794hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg385440
hg195440
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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