A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565655



Internal ID22434371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109499103..109499103hg38UCSC Ensembl
chr9:112261383..112261383hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348317, nssv14348316
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565655
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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