A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674762



Internal ID9940867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138450492..138452475hg38UCSC Ensembl
Outerchr7:138450335..138452628hg38UCSC Ensembl
Innerchr7:138135237..138137220hg19UCSC Ensembl
Outerchr7:138135080..138137373hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241e199
Supporting Variantsessv6043438
SamplesNA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674762
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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