A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423644



Internal ID202660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14370180..14370240hg38UCSC Ensembl
chrX:14388302..14388362hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423644
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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