A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv507407



Internal ID15479086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:106863770..106869770hg38UCSC Ensembl
Outerchr7:106504215..106510215hg19UCSC Ensembl
Outerchr7:106291451..106297451hg18UCSC Ensembl
Outerchr7:106098166..106104166hg17UCSC Ensembl
Cytoband7q22.3
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 Variantsnssv621884, nssv620387
SamplesNA15510, NA10860
Known GenesPIK3CG
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)nsv507407
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