A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999079



Internal ID20566119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40316058..40316713hg38UCSC Ensembl
chr12:40709860..40710515hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462530
Supporting Variants
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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