A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178533



Internal ID20745573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13497595..13505915hg38UCSC Ensembl
chr12:13650529..13658849hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg388321
hg198321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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