A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663653



Internal ID9929758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23370825..23372194hg38UCSC Ensembl
Outerchr7:23370788..23372244hg38UCSC Ensembl
Innerchr7:23410444..23411813hg19UCSC Ensembl
Outerchr7:23410407..23411863hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5907146
SamplesNA19704
Known GenesIGF2BP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663653
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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