A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128886



Internal ID19280780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:14920976..14926776hg38UCSC Ensembl
Outerchr4:14922600..14928400hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961555
SamplesKWS1
Known GenesCPEB2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128886
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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