A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076433



Internal ID19315876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34939528..34962629hg38UCSC Ensembl
chr16:34173899..34197000hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3823102
hg1923102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771746
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076433
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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