A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661827



Internal ID9927932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112670856..112671942hg38UCSC Ensembl
Outerchr13:112670699..112672095hg38UCSC Ensembl
Innerchr13:113325170..113326256hg19UCSC Ensembl
Outerchr13:113325013..113326409hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv381e199
Supporting Variantsessv5420054, essv5843204, essv6114004, essv5412866, essv5395733, essv5620066, essv5810219, essv6035282
SamplesNA19704, NA19819, NA18489, NA19391, NA18853, NA19318, NA18873, NA19900
Known GenesC13orf35
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661827
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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