A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584605



Internal ID20957676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103525168..103525787hg38UCSC Ensembl
chr12:103918946..103919565hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1677n223
Supporting Variantsnssv18225879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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