A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648516



Internal ID21596821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78993266..78993266hg38UCSC Ensembl
chr15:79285608..79285608hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079760
SamplesHG00731
Known GenesRASGRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648516
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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