A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673635



Internal ID9593054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28534679..28535528hg38UCSC Ensembl
chr7:28574297..28575146hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1189e199
Supporting Variantsessv6283107, essv6345156, essv6529508, essv5608438, essv5942370, essv6536309, essv6151195, essv5644124, essv5841224, essv6584910, essv6375189, essv6567570, essv6116733, essv5653366, essv6447810, essv6109743, essv6500481, essv5992504, essv6386548, essv6584581
SamplesNA11830, NA18947, NA11829, NA10851, NA18561, NA18571, NA12761, NA12156, NA11994, NA11831, NA18566, NA18573, NA11919, NA18576, NA12716, NA07051, NA07037, NA06986, NA12154, NA12776
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673635
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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