A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736753



Internal ID160419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46487889..46487889hg38UCSC Ensembl
chrX:46347324..46347324hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736753
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000499251


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