A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085358



Internal ID21994591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105716089..105716089hg38UCSC Ensembl
chr12:106109867..106109867hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg385759
hg195759
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085358
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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