A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993815



Internal ID6729772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132213725..132214038hg38UCSC Ensembl
chr11:132083619..132083932hg19UCSC Ensembl
chr11:131588829..131589142hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38314
hg19314
hg18314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574757
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993815
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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