A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677080



Internal ID9943185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107867747..107869704hg38UCSC Ensembl
Outerchr4:107867710..107869754hg38UCSC Ensembl
Innerchr4:108788903..108790860hg19UCSC Ensembl
Outerchr4:108788866..108790910hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382045
hg192045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6501789
SamplesNA19114
Known GenesSGMS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677080
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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