A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3108n100



Internal ID19013476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15966243..16193927hg38UCSC Ensembl
chr17:15869557..16097241hg19UCSC Ensembl
chr17:15810282..16037966hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38227685
hg19227685
hg18227685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055173, nsv1062220, nsv1064878
Samples
Known GenesADORA2B, NCOR1, TTC19, ZSWIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3108n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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