A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098359



Internal ID22007592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28493756..28493756hg38UCSC Ensembl
chr16:28505077..28505077hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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