A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228747



Internal ID22370830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3477522..3477658hg38UCSC Ensembl
chr16:3527522..3527658hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383411
SamplesHG00513
Known GenesNAA60
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228747
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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