A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586839



Internal ID20959910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54274801..54275495hg38UCSC Ensembl
chr12:54668585..54669279hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223772
Samples
Known GenesCBX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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