A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514437



Internal ID20887790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58647678..58649500hg38UCSC Ensembl
chr16:58681582..58683404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381823
hg191823
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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