A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661537



Internal ID9927642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:198303692..198305362hg38UCSC Ensembl
Outerchr2:198303655..198305412hg38UCSC Ensembl
Innerchr2:199168416..199170086hg19UCSC Ensembl
Outerchr2:199168379..199170136hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6367977
SamplesNA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661537
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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