A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2703n100



Internal ID20154319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6253801..6603812hg38UCSC Ensembl
chr16:6303802..6653813hg19UCSC Ensembl
chr16:6243803..6593814hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38350012
hg19350012
hg18350012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043020, nsv1046604
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)dgv2703n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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