A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279887



Internal ID20489105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76108984..76158472hg38UCSC Ensembl
chr6:76818701..76868189hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3849489
hg1949489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279887
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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