A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv622363



Internal ID15470902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151656762..151740604hg38UCSC Ensembl
Outerchr3:151374550..151458392hg19UCSC Ensembl
Outerchr3:152857240..152941082hg18UCSC Ensembl
Outerchr3:152857248..152941090hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3883843
hg1983843
hg1883843
hg1783843
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511102
Supporting Variants
SamplesNA10860
Known GenesAADACL2, MIR548H2
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)nssv622363
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