A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645909



Internal ID21594214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62073340..62073340hg38UCSC Ensembl
chr12:62467121..62467121hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097821
SamplesNA12878
Known GenesFAM19A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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