A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113833



Internal ID18905627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88967171..88967225hg38UCSC Ensembl
Outerchr16:89033579..89033633hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969910
SamplesKWS2
Known GenesCBFA2T3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113833
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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