A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504662



Internal ID20877925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60598615..60606943hg38UCSC Ensembl
chr16:60632519..60640847hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg388329
hg198329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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