A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557056



Internal ID18508651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6801682..6866450hg38UCSC Ensembl
Innerchr16:6851683..6916451hg19UCSC Ensembl
Innerchr16:6791684..6856452hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3864769
hg1964769
hg1864769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054789
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557056
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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