A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951065



Internal ID17299939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:105042274..105046073hg38UCSC Ensembl
Outerchr11:104913001..104916800hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999612
SamplesBILGI_BIOE
Known GenesCARD16
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951065
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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