A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv618655



Internal ID15816461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166268075..166291064hg38UCSC Ensembl
Outerchr6:166681563..166704552hg19UCSC Ensembl
Outerchr6:166601553..166624542hg18UCSC Ensembl
Outerchr6:166651974..166674963hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3822990
hg1922990
hg1822990
hg1722990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510952
Supporting Variants
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)nssv618655
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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