A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739957



Internal ID163623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33415288..33415339hg38UCSC Ensembl
chrX:33433405..33433456hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739957
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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