A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428528



Internal ID207396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46211373..46267883hg38UCSC Ensembl
chrX:46070808..46127318hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3856511
hg1956511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428528
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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