A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646964



Internal ID21595269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69678416..69678416hg38UCSC Ensembl
chr15:69970755..69970755hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089719
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646964
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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