A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466783



Internal ID21124336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76170290..76178422hg38UCSC Ensembl
chr12:76564070..76572202hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg388133
hg198133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466783
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