A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459520



Internal ID21117073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32382659..32383303hg38UCSC Ensembl
chr12:32535593..32536237hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459520
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