A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671798



Internal ID9937903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164806009..164833780hg38UCSC Ensembl
Outerchr3:164805972..164833830hg38UCSC Ensembl
Innerchr3:164523797..164551568hg19UCSC Ensembl
Outerchr3:164523760..164551618hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3827859
hg1927859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv894e199
Supporting Variantsessv5432470
SamplesNA19904
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671798
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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