A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2709n100



Internal ID19013077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6788872..6866450hg38UCSC Ensembl
chr16:6838873..6916451hg19UCSC Ensembl
chr16:6778874..6856452hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3877579
hg1977579
hg1877579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054789, nsv1049270
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)dgv2709n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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