A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462997



Internal ID21120550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102564677..102565311hg38UCSC Ensembl
chr12:102958455..102959089hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462997
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