A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5551919



Internal ID9358539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111210659..111215615hg38UCSC Ensembl
Outerchr6:111210622..111215665hg38UCSC Ensembl
Innerchr6:111531862..111536818hg19UCSC Ensembl
Outerchr6:111531825..111536868hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661859
Supporting Variants
SamplesNA18553
Known GenesSLC16A10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5551919
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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