A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv507253



Internal ID15823344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:55657448..55663448hg38UCSC Ensembl
Outerchr5:54953276..54959276hg19UCSC Ensembl
Outerchr5:54989033..54995033hg18UCSC Ensembl
Outerchr5:54989033..54995033hg17UCSC Ensembl
Cytoband5q11.2
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 Variantsnssv620296, nssv621790
SamplesNA15510, NA10860
Known GenesSLC38A9
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)nsv507253
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