A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658920



Internal ID9925025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11106286..11107234hg38UCSC Ensembl
Outerchr2:11106129..11107387hg38UCSC Ensembl
Innerchr2:11246412..11247360hg19UCSC Ensembl
Outerchr2:11246255..11247513hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5549703, essv6374468
SamplesNA19391, NA19334
Known GenesFLJ33534
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658920
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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