A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196722



Internal ID20763762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37503375..37507762hg38UCSC Ensembl
chr17:35863481..35867868hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384388
hg194388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499525
Supporting Variants
Samples
Known GenesDUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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