A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075908



Internal ID19321157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1733298..1740499hg38UCSC Ensembl
chr16:1783299..1790500hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387202
hg197202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765323
SamplesKWP1
Known GenesMAPK8IP3, MIR3177
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075908
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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