A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952911



Internal ID16955098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:6019000..6021499hg38UCSC Ensembl
Outerchr16:6069001..6071500hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999208
SamplesBILGI_BIOE
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952911
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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