A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110683



Internal ID18918469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47746532..47746587hg38UCSC Ensembl
Outerchr11:47768084..47768139hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961091
SamplesKWS1
Known GenesFNBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110683
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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