A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2708n100



Internal ID19013076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6740169..6965769hg38UCSC Ensembl
chr16:6790170..7015770hg19UCSC Ensembl
chr16:6730171..6955771hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38225601
hg19225601
hg18225601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053371, nsv1048370, nsv1049393
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)dgv2708n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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