A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142205



Internal ID19275403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87158055..87181768hg38UCSC Ensembl
Outerchr16:87191661..87215374hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3823714
hg1923714
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993716
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142205
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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