A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181762



Internal ID20748802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14836412..14836707hg38UCSC Ensembl
chr12:14989346..14989641hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467435
Supporting Variants
Samples
Known GenesART4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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