A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579806



Internal ID20952877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60379890..60382428hg38UCSC Ensembl
chr12:60773671..60776209hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg382539
hg192539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579806
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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