A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv508012



Internal ID15479688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:46074437..46080437hg38UCSC Ensembl
Outerchr1:46540109..46546109hg19UCSC Ensembl
Outerchr1:46312696..46318696hg18UCSC Ensembl
Outerchr1:46252129..46258129hg17UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621467
SamplesNA15510
Known GenesPIK3R3
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)nsv508012
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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