A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625997



Internal ID7012831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37932633..38000019hg38UCSC Ensembl
chr11:37954183..38021569hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3867387
hg1967387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14095036
SamplesHG03782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625997
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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