A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528120



Internal ID21852477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186857180..186857180hg38UCSC Ensembl
chr1:186826312..186826312hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042685
Supporting Variants
Samples
Known GenesPLA2G4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528120
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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