A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430927



Internal ID209720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23831788..23851425hg38UCSC Ensembl
chrX:23849905..23869542hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3819638
hg1919638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739701
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430927
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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