A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096210



Internal ID22005443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115162016..115162016hg38UCSC Ensembl
chr9:117924295..117924295hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591663
Samples
Known GenesDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096210
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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