A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1108980



Internal ID18930610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:6859124..6859190hg38UCSC Ensembl
Outerchr16:6909125..6909191hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954788
SamplesKWS1
Known GenesRBFOX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1108980
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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