A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659949



Internal ID21608254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97124918..97124918hg38UCSC Ensembl
chr15:97668148..97668148hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082214
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659949
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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