A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664849



Internal ID9930954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178035842..178039332hg38UCSC Ensembl
Outerchr3:178035685..178039485hg38UCSC Ensembl
Innerchr3:177753630..177757120hg19UCSC Ensembl
Outerchr3:177753473..177757273hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5628570
SamplesNA18508
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664849
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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