A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737567



Internal ID161233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130210955..130211059hg38UCSC Ensembl
chrX:129344929..129345033hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426433
Supporting Variants
Samples
Known GenesZNF280C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737567
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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