A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952084



Internal ID17300958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:90214193..90225392hg38UCSC Ensembl
Outerchr16:90280601..90291800hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000203
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952084
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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