A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582080



Internal ID20955151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10210135..10211162hg38UCSC Ensembl
chr12:10362734..10363761hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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