A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603513



Internal ID21552178
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 Variantsnssv17091840
SamplesHG01596
Known GenesRASGRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603513
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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