A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951068



Internal ID17299942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110093675..110105975hg38UCSC Ensembl
Outerchr11:109964401..109976700hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812301
hg1912300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999615
SamplesBILGI_BIOE
Known GenesZC3H12C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951068
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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