A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181056



Internal ID20748096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15968740..16040574hg38UCSC Ensembl
chr12:16121674..16193508hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3871835
hg1971835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471827
Supporting Variants
Samples
Known GenesDERA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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