A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950918



Internal ID16953105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99105819..99122718hg38UCSC Ensembl
Outerchr9:101868101..101885000hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3816900
hg1916900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996949
SamplesBILGI_BIOE
Known GenesTGFBR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950918
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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