A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509621



Internal ID20882932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81035201..81038100hg38UCSC Ensembl
chr16:81068806..81071705hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189416
Samples
Known GenesATMIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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