A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv661n100



Internal ID20152277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3749938..3788015hg38UCSC Ensembl
chr10:3792130..3830207hg19UCSC Ensembl
chr10:3782130..3820207hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3838078
hg1938078
hg1838078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035650, nsv1048831
Samples
Known GenesKLF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv661n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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