A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505581



Internal ID20878852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75683484..75700104hg38UCSC Ensembl
chr16:75717382..75734002hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816621
hg1916621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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