A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6389257



Internal ID9421536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143226922..143236343hg38UCSC Ensembl
Outerchr8:143226765..143236496hg38UCSC Ensembl
Innerchr8:144309092..144318513hg19UCSC Ensembl
Outerchr8:144308935..144318666hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg389732
hg199732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673721
Supporting Variants
SamplesNA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6389257
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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