A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166277



Internal ID21430039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153150697..153249951hg38UCSC Ensembl
chrX:152415432..152514702hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3899255
hg1999271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670532
Supporting Variants
SamplesHG00731
Known GenesMAGEA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166277
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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