A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649310



Internal ID21597615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67954737..67954737hg38UCSC Ensembl
chr12:68348517..68348517hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080345
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649310
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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