A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660685



Internal ID21608990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42188023..42188023hg38UCSC Ensembl
chr15:42480221..42480221hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092515
SamplesHG03125
Known GenesVPS39
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660685
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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