A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576327



Internal ID20949398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98487893..98488194hg38UCSC Ensembl
chr12:98881671..98881972hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229103
Samples
Known GenesLOC643770
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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