A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664842



Internal ID9930947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106326205..106420119hg38UCSC Ensembl
chr1:106868827..106962741hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3893915
hg1993915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5767466
SamplesNA19446
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664842
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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