A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224728



Internal ID22368070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46789380..46802406hg38UCSC Ensembl
chr16:46823292..46836318hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3813027
hg1913027
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390849
SamplesHG00512
Known GenesC16orf87
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224728
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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