A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460317



Internal ID21117870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77688667..77689257hg38UCSC Ensembl
chr12:78082447..78083037hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460317
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