A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591466



Internal ID20964537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:72874121..73065135hg38UCSC Ensembl
chr12:73267901..73458915hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38191015
hg19191015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer