A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272101



Internal ID20839141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89213913..89214230hg38UCSC Ensembl
chr6:89923632..89923949hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557692
Supporting Variants
Samples
Known GenesGABRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.48204


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