A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv718n100



Internal ID22786805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42159342..42357663hg38UCSC Ensembl
chr10:42654790..42853111hg19UCSC Ensembl
chr10:41974796..42173117hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38198322
hg19198322
hg18198322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042015, nsv1035669, nsv1047906
Samples
Known GenesLOC441666
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv718n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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