A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087280



Internal ID21996513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27661935..27661935hg38UCSC Ensembl
chr16:27673256..27673256hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633370
Samples
Known GenesKIAA0556
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087280
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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