A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579041



Internal ID20952112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104161747..104162315hg38UCSC Ensembl
chr12:104555525..104556093hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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