A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954789



Internal ID18865757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:6886250..6886315hg38UCSC Ensembl
Outerchr16:6936251..6936316hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1108981
Supporting Variants
SamplesKWS1
Known GenesRBFOX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954789
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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