A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422406



Internal ID201451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5661030..5661837hg38UCSC Ensembl
chrX:5579071..5579878hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422406
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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