A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738072



Internal ID161738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153405986..153406370hg38UCSC Ensembl
chrX:152671444..152671828hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738072
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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