A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625188



Internal ID7012023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4497992..4570623hg38UCSC Ensembl
chr11:4519222..4591853hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3872632
hg1972632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13998768, essv13998771, essv13998770, essv13998769, essv13998767
SamplesNA18599, HG03844, HG03132, NA18566, NA18624
Known GenesOR52M1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625188
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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