A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625355



Internal ID6665502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10326748..10327580hg38UCSC Ensembl
Innerchr11:10326770..10327559hg38UCSC Ensembl
Outerchr11:10326727..10327602hg38UCSC Ensembl
chr11:10348295..10349127hg19UCSC Ensembl
Innerchr11:10348317..10349106hg19UCSC Ensembl
Outerchr11:10348274..10349149hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14028054, essv14028053, essv14028052
SamplesHG03772, HG03229, HG02494
Known GenesCAND1.11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625355
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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