A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510467



Internal ID15826493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76605763..76611763hg38UCSC Ensembl
Outerchr18:74317720..74323720hg19UCSC Ensembl
Outerchr18:72446708..72452708hg18UCSC Ensembl
Outerchr18:72446708..72452708hg17UCSC Ensembl
Cytoband18q23
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 Variantsnssv618443
SamplesCHM
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)nsv510467
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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