A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590548



Internal ID20963619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64605161..64605681hg38UCSC Ensembl
chr12:64998941..64999461hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1570n223
Supporting Variantsnssv18219330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590548
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