A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611212



Internal ID21559517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176209307..176209307hg38UCSC Ensembl
chr1:176178443..176178443hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061356
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611212
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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