A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090923



Internal ID22000156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79001281..79001281hg38UCSC Ensembl
chr15:79293623..79293623hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602419
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090923
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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