A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580466



Internal ID20953537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126118531..126119349hg38UCSC Ensembl
chr12:126603077..126603895hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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