A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095903



Internal ID22005136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2787293..2787293hg38UCSC Ensembl
chr16:2837294..2837294hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095903
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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