A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509549



Internal ID15477047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100818780..100886836hg38UCSC Ensembl
Outerchr14:101285117..101353173hg19UCSC Ensembl
Outerchr14:100354870..100422926hg18UCSC Ensembl
Outerchr14:100354870..100422926hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383167
hg193167
hg183167
hg173167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv619659
SamplesNA10860
Known GenesMEG3, MIR127, MIR136, MIR337, MIR431, MIR432, MIR433, MIR493, MIR665, MIR770, RTL1
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)nsv509549
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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