A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv202e214



Internal ID22756096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62366510..62385431hg38UCSC Ensembl
chr11:62133982..62152903hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3818922
hg1918922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626602, esv3626601
SamplesNA19704, HG00674, HG02545, NA19834, NA18628
Known GenesASRGL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv202e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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