A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668001



Internal ID9934106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183360584..183366367hg38UCSC Ensembl
Outerchr3:183360547..183366417hg38UCSC Ensembl
Innerchr3:183078372..183084155hg19UCSC Ensembl
Outerchr3:183078335..183084205hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg385871
hg195871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv899e199
Supporting Variantsessv6206703
SamplesNA18602
Known GenesMCF2L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668001
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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