A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv460827



Internal ID15174206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117584524..117729467hg38UCSC Ensembl
Innerchr3:117303371..117448314hg19UCSC Ensembl
Innerchr3:118786061..118931004hg18UCSC Ensembl
Innerchr3:118786061..118931004hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38144944
hg19144944
hg18144944
hg17144944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv537328
SamplesHGDP01361
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)nsv460827
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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