A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123111



Internal ID21486246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1491222..1491222hg38UCSC Ensembl
chr5:1491337..1491337hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640840
Supporting Variants
SamplesNA12878
Known GenesLPCAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123111
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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