A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv621854



Internal ID15819077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99186709..99192709hg38UCSC Ensembl
Outerchr6:99634585..99640585hg19UCSC Ensembl
Outerchr6:99741306..99747306hg18UCSC Ensembl
Outerchr6:99741306..99747306hg17UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv507352
Supporting Variants
SamplesNA10860
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)nssv621854
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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