A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077818



Internal ID19318318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21731078..21745779hg38UCSC Ensembl
chr16:21742399..21757100hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3814702
hg1914702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766668
SamplesKWP1
Known GenesOTOA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077818
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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