A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423826



Internal ID202837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40487608..40517255hg38UCSC Ensembl
chrX:40346860..40376507hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3829648
hg1929648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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