A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511007



Internal ID15827029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101678130..101726065hg38UCSC Ensembl
Outerchr11:101548861..101596796hg19UCSC Ensembl
Outerchr11:101054071..101102006hg18UCSC Ensembl
Outerchr11:101054071..101102006hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3847936
hg1947936
hg1847936
hg1747936
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618619
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)nsv511007
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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