A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951601



Internal ID16953788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:34437654..34452153hg38UCSC Ensembl
Outerchr11:34459201..34473700hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998174
SamplesBILGI_BIOE
Known GenesCAT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951601
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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