A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv467298



Internal ID15180677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65025888..65372541hg38UCSC Ensembl
Innerchr10:66785646..67132299hg19UCSC Ensembl
Innerchr10:66455652..66802305hg18UCSC Ensembl
Innerchr10:66455652..66802305hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38346654
hg19346654
hg18346654
hg17346654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107n27
Supporting Variantsnssv542632
SamplesHGDP00145
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)nsv467298
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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