A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509966



Internal ID15477464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:33666703..33672703hg38UCSC Ensembl
Outerchr5:33666808..33672808hg19UCSC Ensembl
Outerchr5:33702565..33708565hg18UCSC Ensembl
Outerchr5:33702565..33708565hg17UCSC Ensembl
Cytoband5p13.3
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 Variantsnssv618203, nssv622084, nssv623975
SamplesCHM, NA18994, NA10860
Known GenesADAMTS12
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)nsv509966
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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