A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503805



Internal ID20877061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61126701..61130800hg38UCSC Ensembl
chr16:61160605..61164704hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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