A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590952



Internal ID20964023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110969403..110969826hg38UCSC Ensembl
chr12:111407207..111407630hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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