A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036797



Internal ID18779328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6031911..6059326hg38UCSC Ensembl
Innerchr16:6081912..6109327hg19UCSC Ensembl
Innerchr16:6021913..6049328hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827416
hg1927416
hg1827416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557014
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)nsv1036797
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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