A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740059



Internal ID163725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36322376..36341402hg38UCSC Ensembl
chrX:36340491..36359517hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3819027
hg1919027
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562818
Supporting Variants
Samples
Known GenesCXorf30
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740059
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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