A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001364



Internal ID16947630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:41200310..41224409hg38UCSC Ensembl
Outerchr3:41241801..41265900hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3824100
hg1924100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954468
Supporting Variants
SamplesBILGI_BIOE
Known GenesCTNNB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001364
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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