A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6586149



Internal ID9563552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144492586..144495687hg38UCSC Ensembl
chr8:145717969..145721070hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671709
Supporting Variants
SamplesNA20808
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6586149
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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