A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214585



Internal ID22361201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20041132..20041208hg38UCSC Ensembl
chr16:20052454..20052530hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383085, nssv14376382
SamplesHG00731, HG00513
Known GenesGPR139
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214585
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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