A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146422



Internal ID19202677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:91433055..91435956hg38UCSC Ensembl
Outerchr14:91899399..91902300hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999624
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146422
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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