A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736637



Internal ID160303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43715620..43715698hg38UCSC Ensembl
chrX:43574867..43574945hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415851
Supporting Variants
Samples
Known GenesMAOA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736637
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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