A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501672



Internal ID20874909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3442661..3450686hg38UCSC Ensembl
chr16:3492661..3500686hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388026
hg198026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186388
Samples
Known GenesNAA60, ZNF597
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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