A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv706n100



Internal ID20152322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34881487..35230186hg38UCSC Ensembl
chr10:35170415..35519114hg19UCSC Ensembl
chr10:35210421..35559120hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38348700
hg19348700
hg18348700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053665, nsv1046128, nsv1042534
Samples
Known GenesCREM, CUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv706n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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