A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467860



Internal ID22525750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4117454..4117508hg38UCSC Ensembl
chrX:4035495..4035549hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467860
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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