A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189192



Internal ID20756232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68386308..68407867hg38UCSC Ensembl
chr12:68780088..68801647hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3821560
hg1921560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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