A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579488



Internal ID20952559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96066298..96067681hg38UCSC Ensembl
chr12:96460076..96461459hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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