A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082730



Internal ID21991963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58395903..58395903hg38UCSC Ensembl
chr16:58429807..58429807hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635225
Samples
Known GenesGINS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082730
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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