A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497289



Internal ID20870495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81018361..81105943hg38UCSC Ensembl
chr16:81051966..81139548hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3887583
hg1987583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181898
Samples
Known GenesATMIN, C16orf46, CENPN, GCSH, PKD1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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