A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2716n100



Internal ID19013084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7162338..7193774hg38UCSC Ensembl
chr16:7212339..7243775hg19UCSC Ensembl
chr16:7152340..7183776hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831437
hg1931437
hg1831437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053518, nsv1043009, nsv1039050
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)dgv2716n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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