A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626160



Internal ID6666309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44279795..44284852hg38UCSC Ensembl
Innerchr11:44279795..44284852hg38UCSC Ensembl
Outerchr11:44279616..44285027hg38UCSC Ensembl
chr11:44301345..44306402hg19UCSC Ensembl
Innerchr11:44301345..44306402hg19UCSC Ensembl
Outerchr11:44301166..44306577hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385058
hg195058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116448, essv14116447
SamplesHG01402, NA20287
Known GenesALX4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626160
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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