A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510391



Internal ID15826417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25593462..25599462hg38UCSC Ensembl
Outerchr15:25838609..25844609hg19UCSC Ensembl
Outerchr15:23389702..23395702hg18UCSC Ensembl
Outerchr15:23389702..23395702hg17UCSC Ensembl
Cytoband15q12
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 Variantsnssv621419
SamplesNA15510
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)nsv510391
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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