A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415466



Internal ID194723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46504601..46505173hg38UCSC Ensembl
chrX:46364036..46364608hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736757
Samples
Known GenesZNF674
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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