A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092155



Internal ID22001388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94984148..94984148hg38UCSC Ensembl
chr10:96743905..96743905hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581062
Samples
Known GenesCYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092155
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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