A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv709n100



Internal ID22786796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38356896..38780907hg38UCSC Ensembl
chr10:38645824..39074038hg19UCSC Ensembl
chr10:38685830..39114044hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38424012
hg19428215
hg18428215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052697, nsv1043781, nsv1036840, nsv1048953
Samples
Known GenesACTR3BP5, HSD17B7P2, LINC00999, SEPT7P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv709n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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