A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997342



Internal ID19187299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:111103677..111103751hg38UCSC Ensembl
Outerchr11:110974401..110974475hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145977
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997342
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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