A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616779



Internal ID7003665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29919111..29925745hg38UCSC Ensembl
Innerchr8:29919117..29925739hg38UCSC Ensembl
Outerchr8:29919105..29925751hg38UCSC Ensembl
chr8:29776627..29783261hg19UCSC Ensembl
Innerchr8:29776633..29783255hg19UCSC Ensembl
Outerchr8:29776621..29783267hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386635
hg196635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13153656
SamplesHG00378
Known GenesFAM183CP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616779
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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