A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677846



Internal ID9943951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236754842..236771710hg38UCSC Ensembl
Outerchr2:236754791..236771760hg38UCSC Ensembl
Innerchr2:237663485..237680353hg19UCSC Ensembl
Outerchr2:237663434..237680403hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3816970
hg1916970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5579329
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677846
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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