A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386588



Internal ID22196353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99790836..99790836hg38UCSC Ensembl
chr15:100331041..100331041hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560489
Supporting Variants
SamplesHG00731
Known GenesDNM1P46
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14386588
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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