A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115513



Internal ID19284399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:90125492..90225992hg38UCSC Ensembl
Outerchr16:90191900..90292400hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38100501
hg19100501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977321
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115513
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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