A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148411



Internal ID19201915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:34160132..34196333hg38UCSC Ensembl
Outerchr16:33962599..33998800hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3836202
hg1936202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000451
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148411
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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