A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463017



Internal ID22520902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35800152..35818113hg38UCSC Ensembl
chrX:35818269..35836230hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3817962
hg1917962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877414
Supporting Variants
Samples
Known GenesMAGEB16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463017
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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