A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953555



Internal ID17302429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:62919268..62955467hg38UCSC Ensembl
Outerchr18:60586501..60622700hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3836200
hg1936200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998890
SamplesBILGI_BIOE
Known GenesPHLPP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953555
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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