A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462658



Internal ID22520543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2448583..2470962hg38UCSC Ensembl
chrX:2366624..2389003hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3822380
hg1922380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880541
Supporting Variants
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462658
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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