A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178012



Internal ID20745052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15613018..15618678hg38UCSC Ensembl
chr12:15765952..15771612hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385661
hg195661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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