A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660954



Internal ID9927059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11037592..11046208hg38UCSC Ensembl
Outerchr1:11037555..11046258hg38UCSC Ensembl
Innerchr1:11097649..11106265hg19UCSC Ensembl
Outerchr1:11097612..11106315hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388704
hg198704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5962966
SamplesNA19257
Known GenesMASP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660954
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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