A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509581



Internal ID15477079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88514213..88597724hg38UCSC Ensembl
Outerchr15:89057444..89140955hg19UCSC Ensembl
Outerchr15:86858448..86941959hg18UCSC Ensembl
Outerchr15:86858448..86941959hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384403
hg194403
hg184403
hg174403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621015
SamplesNA15510
Known GenesDET1
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)nsv509581
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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