A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470465



Internal ID21128018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49321640..49322257hg38UCSC Ensembl
chr12:49715423..49716040hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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