A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949786



Internal ID16951973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8619374..8635674hg38UCSC Ensembl
Outerchr4:8621101..8637400hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3816301
hg1916300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996658
SamplesBILGI_BIOE
Known GenesCPZ
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949786
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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