A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097848



Internal ID22007081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18179110..18179110hg38UCSC Ensembl
chr10:18468039..18468039hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582273
Samples
Known GenesCACNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097848
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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