A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644089



Internal ID21592394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29407556..29407556hg38UCSC Ensembl
chr8:29265073..29265073hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156993
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644089
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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