A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098353



Internal ID22007586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98800675..98800675hg38UCSC Ensembl
chr12:99194453..99194453hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606736
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098353
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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