A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736640



Internal ID160306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43771642..43771693hg38UCSC Ensembl
chrX:43630889..43630940hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563362
Supporting Variants
Samples
Known GenesMAOB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736640
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001095


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