A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098887



Internal ID22008120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:397667..397667hg38UCSC Ensembl
chr16:447667..447667hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605410
Samples
Known GenesNME4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098887
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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