A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467434



Internal ID22525325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3326168..3326168hg38UCSC Ensembl
chrX:3244209..3244209hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966790
Supporting Variants
Samples
Known GenesMXRA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467434
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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