A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668434



Internal ID9934539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82257282..82264389hg38UCSC Ensembl
chr9:84872197..84879304hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387108
hg197108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1354e199
Supporting Variantsessv6592685
SamplesNA19651
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668434
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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