A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv459110



Internal ID15519175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682124..18706106hg38UCSC Ensembl
Innerchr21:20054442..20078424hg19UCSC Ensembl
Innerchr21:18976313..19000295hg18UCSC Ensembl
Innerchr21:18976313..19000295hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823983
hg1923983
hg1823983
hg1723983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv524n27
Supporting Variantsnssv535934
SamplesHGDP00641
Known Genes
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv459110
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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