A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193533



Internal ID20760573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10246980..10248725hg38UCSC Ensembl
chr12:10399579..10401324hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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