A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039979



Internal ID21949322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79001281..79001359hg38UCSC Ensembl
chr15:79293623..79293701hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607178
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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