A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146392



Internal ID18852049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14326781..14327087hg38UCSC Ensembl
Outerchr11:14348327..14348633hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999595
SamplesKWB1
Known GenesRRAS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146392
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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