A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998937



Internal ID19194263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:39165331..39165413hg38UCSC Ensembl
Outerchr11:39186881..39186963hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151754
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998937
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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