A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184973



Internal ID20752013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6375376..6385233hg38UCSC Ensembl
chr17:6278696..6288553hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg389858
hg199858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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