A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420959



Internal ID200048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21699521..21699580hg38UCSC Ensembl
chrX:21717639..21717698hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420959
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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