A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272134



Internal ID20839174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9024141..9290888hg38UCSC Ensembl
chr6:9024374..9291121hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38266748
hg19266748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272134
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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