A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944583



Internal ID22720050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79001261..79001339hg38UCSC Ensembl
chr15:79293603..79293681hg19UCSC 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 Variantsnssv17378279
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944583
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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