A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586154



Internal ID20959225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92269307..92270021hg38UCSC Ensembl
chr12:92663083..92663797hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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