A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593752



Internal ID20966823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45482843..45483458hg38UCSC Ensembl
chr12:45876626..45877241hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1532n223
Supporting Variantsnssv18234604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593752
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