A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951069



Internal ID17299943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:111030077..111034476hg38UCSC Ensembl
Outerchr11:110900801..110905200hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999616
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951069
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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