A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644312



Internal ID21836359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23834217..23834337hg38UCSC Ensembl
chrX:23852334..23852454hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101900
Supporting Variants
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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