A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625354



Internal ID6665501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10301318..10303445hg38UCSC Ensembl
Innerchr11:10301354..10303410hg38UCSC Ensembl
Outerchr11:10301283..10303481hg38UCSC Ensembl
chr11:10322865..10324992hg19UCSC Ensembl
Innerchr11:10322901..10324957hg19UCSC Ensembl
Outerchr11:10322830..10325028hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14028051
SamplesHG01917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625354
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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