A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3149853



Internal ID11169519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44721627..44721695hg38UCSC Ensembl
chr11:44743177..44743245hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7419420
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3149853
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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