A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528841



Internal ID22398233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58993765..58994252hg38UCSC Ensembl
chr16:59027669..59028156hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3238n152
Supporting Variantsnssv14377293, nssv14387166, nssv14383848
SamplesHG00512, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528841
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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