A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3110n100



Internal ID22789197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18375163..18571320hg38UCSC Ensembl
chr17:18278477..18474634hg19UCSC Ensembl
chr17:18219202..18415359hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38196158
hg19196158
hg18196158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065690, nsv1062890, nsv1056902, nsv1062985, nsv1067238, nsv1063814, nsv1058895, nsv1067496, nsv1061073, nsv1064293
Samples
Known GenesCCDC144B, EVPLL, FAM106A, FLJ35934, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3110n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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