A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586746



Internal ID20959817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131309444..131651986hg38UCSC Ensembl
chr12:131793989..132136531hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38342543
hg19342543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n223
Supporting Variantsnssv18219692
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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