A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040296



Internal ID18782827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6814336..6877384hg38UCSC Ensembl
Innerchr16:6864337..6927385hg19UCSC Ensembl
Innerchr16:6804338..6867386hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3863049
hg1963049
hg1863049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2710n100
Supporting Variantsnssv3557058
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)nsv1040296
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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