A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998151



Internal ID16944417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:13008654..13011453hg38UCSC Ensembl
Outerchr11:13030201..13033000hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951309
Supporting Variants
SamplesBILGI_BIOE
Known GenesRASSF10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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