A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557921



Internal ID20930992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139105352..139107195hg38UCSC Ensembl
chr6:139426489..139428332hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557921
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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