A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668707



Internal ID9934812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707298..52707410hg38UCSC Ensembl
chr13:53281433..53281545hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6382106, essv5840517, essv5469307, essv6362385, essv5519040, essv5815146, essv6476078, essv5528171, essv6547064, essv5689047
SamplesNA12717, NA18592, NA18603, NA18545, NA12761, NA18537, NA18570, NA18564, NA07051, NA18609
Known GenesLECT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668707
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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