A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510061



Internal ID15826087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165390830..165396830hg38UCSC Ensembl
Outerchr6:165804319..165810319hg19UCSC Ensembl
Outerchr6:165724309..165730309hg18UCSC Ensembl
Outerchr6:165774730..165780730hg17UCSC Ensembl
Cytoband6q27
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 Variantsnssv624020
SamplesNA18994
Known GenesPDE10A
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)nsv510061
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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