A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593951



Internal ID20967022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105345201..105345596hg38UCSC Ensembl
chr12:105738979..105739374hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223754
Samples
Known GenesC12orf75
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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