A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148667



Internal ID19196086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21729978..21793879hg38UCSC Ensembl
Outerchr16:21741299..21805200hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3863902
hg1963902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997452
SamplesKWB1
Known GenesOTOA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148667
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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