A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426788



Internal ID205707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68562542..68579871hg38UCSC Ensembl
chrX:67782384..67799713hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3817330
hg1917330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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