A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180396



Internal ID20747436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21419932..21705830hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38285899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00147


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