A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765171



Internal ID18960688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6692698..6693999hg38UCSC Ensembl
chr16:6742699..6744000hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075909
Supporting Variants
SamplesKWP1
Known GenesRBFOX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765171
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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