A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607668



Internal ID21555973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45212500..45212500hg38UCSC Ensembl
chr1:45678172..45678172hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3813689
hg1913689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065833
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607668
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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