A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078091



Internal ID18973170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132377112..132378613hg38UCSC Ensembl
chr9:135252499..135254000hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769823
SamplesKWP1
Known GenesTTF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078091
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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