A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594460



Internal ID20967531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51037013..51037761hg38UCSC Ensembl
chr12:51430796..51431544hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594460
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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