A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269819



Internal ID20836859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107960804..107961332hg38UCSC Ensembl
chr6:108282008..108282536hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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