A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661402



Internal ID4705736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16439218..16439506hg19UCSC Ensembl
Outerchr7:16439181..16439556hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv5912579
SamplesNA18989
Known GenesISPD
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661402
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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