A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv507884



Internal ID15823914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:75378473..75384473hg38UCSC Ensembl
Outerchr18:73090428..73096428hg19UCSC Ensembl
Outerchr18:71219416..71225416hg18UCSC Ensembl
Outerchr18:71219416..71225416hg17UCSC Ensembl
Cytoband18q22.3
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 Variantsnssv620635, nssv619210, nssv623253
SamplesNA15510, NA18994, NA10860
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)nsv507884
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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