A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14363632



Internal ID22117282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46213375..46213375hg38UCSC Ensembl
chr1:46679047..46679047hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561666
Supporting Variants
SamplesHG00512
Known GenesLURAP1, POMGNT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14363632
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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