A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088235



Internal ID21997468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3469698..3469698hg38UCSC Ensembl
chr16:3519698..3519698hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613333
Samples
Known GenesNAA60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088235
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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