A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039567



Internal ID18782098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6814336..6878433hg38UCSC Ensembl
Innerchr16:6864337..6928434hg19UCSC Ensembl
Innerchr16:6804338..6868435hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3864098
hg1964098
hg1864098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2710n100
Supporting Variantsnssv3557059
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)nsv1039567
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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