A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077339



Internal ID18970607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32744493..32747194hg38UCSC Ensembl
chr19:33235399..33238100hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771140
SamplesKWP1
Known GenesTDRD12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077339
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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