A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178006



Internal ID20745046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28446412..28551495hg38UCSC Ensembl
chr14:28915618..29020701hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38105084
hg19105084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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