A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098962



Internal ID22008195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100294760..100294760hg38UCSC Ensembl
chr12:100688538..100688538hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598627
Samples
Known GenesSCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098962
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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