A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219075



Internal ID22364210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85555201..85556400hg38UCSC Ensembl
chr16:85588807..85590006hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386223, nssv14391961, nssv14376326, nssv14373057, nssv14387405, nssv14377796, nssv14375004, nssv14380512, nssv14385521
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219075
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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