A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514457



Internal ID20887810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21434296..21720188hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38285893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3034n223
Supporting Variantsnssv18195290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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