A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094886



Internal ID22004119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37246251..37246251hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094886
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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