A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593066



Internal ID20966137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110187268..110188360hg38UCSC Ensembl
chr12:110625073..110626165hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233161
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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