A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585020



Internal ID20958091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80235176..80237121hg38UCSC Ensembl
chr12:80628956..80630901hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220151
Samples
Known GenesOTOGL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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