A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147129



Internal ID21450911
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 StatusS
Merged Variantsnsv5669204
Supporting Variants
SamplesHG01505
Known GenesATXN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147129
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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