A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098026



Internal ID22007259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42008087..42008087hg38UCSC Ensembl
chr12:42401889..42401889hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098026
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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