A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433195



Internal ID211920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115939244..115969853hg38UCSC Ensembl
chrX:115055577..115086186hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3830610
hg1930610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433195
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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