A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5805357



Internal ID8782760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12514422..12516808hg38UCSC Ensembl
Outerchr10:12514265..12516961hg38UCSC Ensembl
Innerchr10:12556421..12558807hg19UCSC Ensembl
Outerchr10:12556264..12558960hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382697
hg192697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666513
Supporting Variants
SamplesNA18637
Known GenesCAMK1D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5805357
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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