A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647437



Internal ID21595742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25674560..25674560hg38UCSC Ensembl
chr12:25827494..25827494hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079568
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647437
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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