A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739702



Internal ID163368
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 StatusS
Merged Variantsnsv5428007
Supporting Variants
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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