A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645883



Internal ID21594188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85879483..85879483hg38UCSC Ensembl
chr12:86273261..86273261hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086051
SamplesHG00732
Known GenesNTS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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