A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740130



Internal ID163796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53902900..53912000hg38UCSC Ensembl
chrX:53929320..53938430hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg389101
hg199111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740130
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000835771


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