A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv664n100



Internal ID20152280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5500146..5577978hg38UCSC Ensembl
chr10:5542109..5619941hg19UCSC Ensembl
chr10:5532109..5609941hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877833
hg1977833
hg1877833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038479, nsv1049523, nsv1052002
Samples
Known GenesCALML3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv664n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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