A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663669



Internal ID9929774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101467309..101467658hg38UCSC Ensembl
chr7:101110590..101110939hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6478473, essv6181602, essv6503378, essv5510607, essv5793569, essv6580164, essv6389942, essv6085461, essv6530975, essv6217375, essv5928601, essv5677842, essv6516021, essv5555334, essv6423576, essv6034736, essv6572931
SamplesNA19703, HG00249, HG00306, HG01140, HG00327, HG00247, NA12156, HG00273, NA11919, HG01334, NA11881, HG00336, HG01137, NA19716, HG00280, HG01061, NA19431
Known GenesCOL26A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663669
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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