A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270542



Internal ID20837582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30596084..30596341hg38UCSC Ensembl
chr6:30563861..30564118hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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