A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588761



Internal ID20961832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110839938..110840316hg38UCSC Ensembl
chr12:111277742..111278120hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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