A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166282



Internal ID21507591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153294977..153328632hg38UCSC Ensembl
chrX:152560435..152594090hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3833656
hg1933656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666818
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166282
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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