A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464890



Internal ID21122443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9876369..9878057hg38UCSC Ensembl
chr12:10028968..10030656hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464890
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