A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv675n100



Internal ID20152291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12469909..12493057hg38UCSC Ensembl
chr10:12511908..12535056hg19UCSC Ensembl
chr10:12551914..12575062hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3823149
hg1923149
hg1823149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036247, nsv1049875
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)dgv675n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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