A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625946



Internal ID7012780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36066286..36087625hg38UCSC Ensembl
chr11:36087836..36109175hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821340
hg1921340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv190e214
Supporting Variantsessv14090629, essv14090628, essv14090627
SamplesNA19020, NA19471, HG03928
Known GenesLDLRAD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625946
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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