A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996893



Internal ID17289845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65661445..65682444hg38UCSC Ensembl
Outerchr9:70483601..70504600hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951514
Supporting Variants
SamplesBILGI_BIOE
Known GenesCBWD3, CBWD5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996893
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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