A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662167



Internal ID9581586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113665925..113666143hg38UCSC Ensembl
Outerchr13:113665888..113666193hg38UCSC Ensembl
Innerchr13:114320240..114320458hg19UCSC Ensembl
Outerchr13:114320203..114320508hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6493615, essv6093402, essv5915954
SamplesNA18592, HG00693, HG00556
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662167
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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