A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510986



Internal ID15827008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:129725541..129755319hg38UCSC Ensembl
Outerchr8:130737787..130767565hg19UCSC Ensembl
Outerchr8:130806969..130836747hg18UCSC Ensembl
Outerchr8:130806969..130836747hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3829779
hg1929779
hg1829779
hg1729779
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618664
SamplesCHM
Known GenesGSDMC
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)nsv510986
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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