A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423835



Internal ID202845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121920728..121938989hg38UCSC Ensembl
chrX:121054581..121072842hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3818262
hg1918262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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