A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582365



Internal ID20955436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121585307..121585566hg38UCSC Ensembl
chr12:122023212..122023471hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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