A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644794



Internal ID21593099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47796754..47796754hg38UCSC Ensembl
chr15:48088951..48088951hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080860
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644794
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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