A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577795



Internal ID20950866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110517582..110519249hg38UCSC Ensembl
chr12:110955387..110957054hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381668
hg191668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227939
Samples
Known GenesRAD9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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