A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092695



Internal ID22001928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112574878..112574878hg38UCSC Ensembl
chr12:113012682..113012682hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092695
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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