A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14028053



Internal ID4029869
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625355
Supporting Variants
SamplesHG03229
Known GenesCAND1.11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14028053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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