A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659903



Internal ID21608208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53226289..53226289hg38UCSC Ensembl
chr12:53620073..53620073hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089988
SamplesHG03125
Known GenesRARG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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