A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357385



Internal ID22142575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24219065..24219065hg38UCSC Ensembl
chr1:24545555..24545555hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561682
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357385
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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