A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv621139



Internal ID15820489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7730150..7845746hg38UCSC Ensembl
Outerchr11:7751697..7867293hg19UCSC Ensembl
Outerchr11:7708273..7823869hg18UCSC Ensembl
Outerchr11:7708273..7823869hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384326
hg194326
hg184326
hg174326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv509387
Supporting Variants
SamplesNA15510
Known GenesOR5P2, OR5P3
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)nssv621139
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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