A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649091



Internal ID21597396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105385610..105385610hg38UCSC Ensembl
chr12:105779388..105779388hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076918
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649091
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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