A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185209



Internal ID20752249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28230518..28238869hg38UCSC Ensembl
chr17:26557544..26565895hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388352
hg198352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185209
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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