A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482516



Internal ID21140069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119889232..119892232hg38UCSC Ensembl
chr12:120327036..120330036hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg383001
hg193001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482516
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