A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527821



Internal ID22397208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24479267..24479343hg38UCSC Ensembl
chr16:24490588..24490664hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384769, nssv14388037, nssv14391800
SamplesNA19238, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527821
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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