A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566247



Internal ID20939318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49263424..49288790hg38UCSC Ensembl
chr6:49231068..49256430hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3825367
hg1925363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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