A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496407



Internal ID20869609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71458453..71470171hg38UCSC Ensembl
chr16:71492356..71504074hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3811719
hg1911719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177127
Samples
Known GenesZNF23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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