A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870307



Internal ID22645243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3329166..3329277hg38UCSC Ensembl
chrX:3247207..3247318hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452015
Samples
Known GenesMXRA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870307
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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