A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559298



Internal ID22428102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79165939..79165939hg38UCSC Ensembl
chr10:80925696..80925696hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354998, nssv14354999
SamplesNA19239, HG00732
Known GenesZMIZ1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559298
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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