A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509256



Internal ID20882564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34596189..34696880hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38100692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2836n223
Supporting Variantsnssv18180246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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