A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182139



Internal ID20749179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51323851..51333763hg38UCSC Ensembl
chr17:49401212..49411124hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg389913
hg199913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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