A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272432



Internal ID20839472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13764769..13765587hg38UCSC Ensembl
chr6:13765001..13765819hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272432
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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