A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999641



Internal ID16945907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:128491006..128505905hg38UCSC Ensembl
Outerchr11:128360901..128375800hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3814900
hg1914900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952758
Supporting Variants
SamplesBILGI_BIOE
Known GenesETS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999641
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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