A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738186



Internal ID161852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155184714..155199247hg38UCSC Ensembl
chrX:154412989..154427524hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814534
hg1914536
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738186
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004059


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