A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511061



Internal ID15827083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:15036920..15111570hg38UCSC Ensembl
Outerchr18:15036919..15111569hg19UCSC Ensembl
Outerchr18:15026919..15101569hg18UCSC Ensembl
Outerchr18:15026919..15101569hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3874651
hg1974651
hg1874651
hg1774651
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621642
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)nsv511061
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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