A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587066



Internal ID20960137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110472749..110473544hg38UCSC Ensembl
chr12:110910554..110911349hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232006
Samples
Known GenesFAM216A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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