A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190409



Internal ID20757450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60193393..60193891hg38UCSC Ensembl
chr14:60660111..60660609hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190409
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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