A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2727n100



Internal ID20154343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9914166..10436036hg38UCSC Ensembl
chr16:10008023..10529893hg19UCSC Ensembl
chr16:9915524..10437394hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38521871
hg19521871
hg18521871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037001, nsv1037707, nsv1042727
Samples
Known GenesATF7IP2, GRIN2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2727n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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