A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576569



Internal ID20949640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113342564..113343053hg38UCSC Ensembl
chr12:113780369..113780858hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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