A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182882



Internal ID20749922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10058781..10059689hg38UCSC Ensembl
chr12:10211380..10212288hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464725
Supporting Variants
Samples
Known GenesCLEC9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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