A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659119



Internal ID4703453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16247638..16330912hg19UCSC Ensembl
Outerchr7:16247601..16330962hg19UCSC 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 Variantsessv5461504
SamplesNA18621
Known GenesISPD, LOC100506025
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659119
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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