A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583720



Internal ID20956791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112414914..112416190hg38UCSC Ensembl
chr12:112852718..112853994hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583720
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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