A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096317



Internal ID22005550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43791148..43791148hg38UCSC Ensembl
chr12:44184951..44184951hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096317
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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