A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2990n100



Internal ID22789077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58344491..58387412hg38UCSC Ensembl
chr16:58378395..58421316hg19UCSC Ensembl
chr16:56935896..56978817hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3842922
hg1942922
hg1842922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058920, nsv1065438, nsv1060471
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)dgv2990n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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