A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582912



Internal ID20955983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14363232..14364278hg38UCSC Ensembl
chr12:14516166..14517212hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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