A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583698



Internal ID20956769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45603815..45604318hg38UCSC Ensembl
chr12:45997598..45998101hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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