A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593040



Internal ID20966111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45144437..45144866hg38UCSC Ensembl
chr12:45538220..45538649hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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