A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565326



Internal ID22434047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94491159..94491159hg38UCSC Ensembl
chr8:95503387..95503387hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342796, nssv14342797
SamplesNA19240, HG00514
Known GenesKIAA1429
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565326
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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