A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2698n100



Internal ID20154314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5304641..5327717hg38UCSC Ensembl
chr16:5354642..5377718hg19UCSC Ensembl
chr16:5294643..5317719hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3823077
hg1923077
hg1823077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041660, nsv1053090
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2698n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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