A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565484



Internal ID22434203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73340327..73340327hg38UCSC Ensembl
chr8:74252562..74252562hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343159
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565484
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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