A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140065



Internal ID21512730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89213913..89214212hg38UCSC Ensembl
chr6:89923632..89923931hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664653
Supporting Variants
Samples
Known GenesGABRR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140065
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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