A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510907



Internal ID15826929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:133015189..133033932hg38UCSC Ensembl
Outerchr6:133336328..133355071hg19UCSC Ensembl
Outerchr6:133378021..133396764hg18UCSC Ensembl
Outerchr6:133378021..133396764hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3818744
hg1918744
hg1818744
hg1718744
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618692
SamplesCHM
Known Genes
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)nsv510907
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer