A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196340



Internal ID20763380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90499849..90512310hg38UCSC Ensembl
chr12:90893626..90906087hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3812462
hg1912462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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