A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511669



Internal ID20884999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68602430..68621198hg38UCSC Ensembl
chr16:68636333..68655101hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3818769
hg1918769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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