A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657164



Internal ID21605469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112031922..112031922hg38UCSC Ensembl
chr12:112469726..112469726hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077195
SamplesNA18534
Known GenesNAA25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657164
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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