A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv676n100



Internal ID20152292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12538413..12555491hg38UCSC Ensembl
chr10:12580412..12597490hg19UCSC Ensembl
chr10:12620418..12637496hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817079
hg1917079
hg1817079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050994, nsv1045242
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv676n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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