A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945350



Internal ID22720826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78970478..78970926hg38UCSC Ensembl
chr15:79262820..79263268hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375109
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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