A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097202



Internal ID21401243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78993001..78993001hg38UCSC Ensembl
chr15:79285343..79285343hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645160
Supporting Variants
SamplesHG00096
Known GenesRASGRF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097202
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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