A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996667



Internal ID20563708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10056209..10061076hg38UCSC Ensembl
chr12:10208808..10213675hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg384868
hg194868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457187
Supporting Variants
Samples
Known GenesCLEC9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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