A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080845



Internal ID21990078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4797627..4797627hg38UCSC Ensembl
chr16:4847628..4847628hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609773
Samples
Known GenesROGDI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080845
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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