A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428007



Internal ID206890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23836220..23838540hg38UCSC Ensembl
chrX:23854337..23856657hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg382321
hg192321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739702
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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