A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426145



Internal ID205087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52206964..52219000hg38UCSC Ensembl
chrX:51950091..51962127hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3812037
hg1912037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426145
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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