A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739705



Internal ID163371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23875632..23892527hg38UCSC Ensembl
chrX:23893749..23910644hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3816896
hg1916896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430218
Supporting Variants
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739705
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00229071


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