A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954880



Internal ID17303753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71060050..71068549hg38UCSC Ensembl
Outerchr3:71109201..71117700hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001408
SamplesBILGI_BIOE
Known GenesFOXP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954880
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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