A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661775



Internal ID9927880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112178460..112178600hg38UCSC Ensembl
Outerchr13:112178423..112178650hg38UCSC Ensembl
Innerchr13:112832774..112832914hg19UCSC Ensembl
Outerchr13:112832737..112832964hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6328582, essv6570366, essv5552300, essv5910026, essv5851841, essv5945465, essv5618064
SamplesHG01051, NA19381, NA19138, NA18557, HG01048, NA18523, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661775
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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