A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954477



Internal ID16956664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45851909..45860208hg38UCSC Ensembl
Outerchr3:45893401..45901700hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001373
SamplesBILGI_BIOE
Known GenesLZTFL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954477
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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