A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078911



Internal ID18969729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15271876..15271962hg38UCSC Ensembl
Outerchr19:15382687..15382773hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762358
SamplesKWP1
Known GenesBRD4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078911
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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