A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098934



Internal ID22008167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104087470..104087470hg38UCSC Ensembl
chr12:104481248..104481248hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609574
Samples
Known GenesHCFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098934
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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