A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568715



Internal ID20941786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32993962..32995091hg38UCSC Ensembl
chr6:32961739..32962868hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381130
hg191130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568715
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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