A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506826



Internal ID20880112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10258217..10308310hg38UCSC Ensembl
chr16:10352074..10402167hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3850094
hg1950094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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