A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594905



Internal ID20967976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79594741..79595564hg38UCSC Ensembl
chr12:79988521..79989344hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233354
Samples
Known GenesPAWR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594905
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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