A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617085



Internal ID21565390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186912706..186912706hg38UCSC Ensembl
chr1:186881838..186881838hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061665
SamplesNA19239
Known GenesPLA2G4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617085
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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