A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv508632



Internal ID15480308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55594098..55680216hg38UCSC Ensembl
Outerchr11:55361574..55447692hg19UCSC Ensembl
Outerchr11:55118150..55204268hg18UCSC Ensembl
Outerchr11:55118150..55204268hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3886119
hg1986119
hg1886119
hg1786119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv619926
SamplesNA15510
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nsv508632
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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