A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2809n100



Internal ID19013177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21577455..21776185hg38UCSC Ensembl
chr16:21588776..21787506hg19UCSC Ensembl
chr16:21496277..21695007hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38198731
hg19198731
hg18198731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043170, nsv1045685, nsv1052153
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2809n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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