A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669204



Internal ID21617509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16741326..16748530hg38UCSC Ensembl
chr6:16741557..16748761hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387205
hg197205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147129
SamplesHG01505
Known GenesATXN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669204
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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