A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095418



Internal ID22004651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37255329..37255329hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382795
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095418
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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