A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736641



Internal ID160307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43809961..43810268hg38UCSC Ensembl
chrX:43669208..43669515hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418860
Supporting Variants
Samples
Known GenesMAOB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736641
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.039963


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