A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891758



Internal ID18839468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12484551..12498801hg38UCSC Ensembl
Outerchr10:12484551..12498801hg38UCSC Ensembl
Innerchr10:12526550..12540800hg19UCSC Ensembl
Outerchr10:12526550..12540800hg19UCSC Ensembl
Innerchr10:12566556..12580806hg18UCSC Ensembl
Outerchr10:12566556..12580806hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3814251
hg1914251
hg1814251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797256
Samples
Known GenesCAMK1D
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891758
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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