A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086384



Internal ID21995617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88831628..88831628hg38UCSC Ensembl
chr16:88898036..88898036hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621382
Samples
Known GenesGALNS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086384
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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