A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455635



Internal ID21113188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92053203..92087741hg38UCSC Ensembl
chr12:92446979..92481517hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3834539
hg1934539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178542
Samples
Known GenesC12orf79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455635
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer