A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077831



Internal ID18970795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70121096..70167197hg38UCSC Ensembl
chr16:70154999..70201100hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3846102
hg1946102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762489
SamplesKWP1
Known GenesPDPR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077831
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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