A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510663



Internal ID15826687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:59018477..59077842hg38UCSC Ensembl
Outerchr15:59310676..59370041hg19UCSC Ensembl
Outerchr15:57097968..57157333hg18UCSC Ensembl
Outerchr15:57097968..57157333hg17UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3859366
hg1959366
hg1859366
hg1759366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618927
SamplesNA10860
Known GenesRNF111
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)nsv510663
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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