A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999606



Internal ID16945872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94545635..94552434hg38UCSC Ensembl
Outerchr11:94278801..94285600hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951059
Supporting Variants
SamplesBILGI_BIOE
Known GenesFUT4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999606
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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