A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097397



Internal ID22006630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75884017..75884017hg38UCSC Ensembl
chr12:76277797..76277797hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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