A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671361



Internal ID9937466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152522995..152525286hg38UCSC Ensembl
Outerchr1:152522838..152525439hg38UCSC Ensembl
Innerchr1:152495471..152497762hg19UCSC Ensembl
Outerchr1:152495314..152497915hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv70e199
Supporting Variantsessv5966732
SamplesNA19921
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671361
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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