A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076459



Internal ID19319128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:84799..120700hg38UCSC Ensembl
chr19:84799..120700hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3835902
hg1935902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764981
SamplesKWP1
Known GenesOR4F17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076459
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer