A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560323



Internal ID22429120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101100906..101100906hg38UCSC Ensembl
chr14:101567243..101567243hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381954
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560323
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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