A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv458284



Internal ID15518349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71183498..71241115hg38UCSC Ensembl
Innerchr18:68850734..68908351hg19UCSC Ensembl
Innerchr18:67001714..67059331hg18UCSC Ensembl
Innerchr18:67001714..67059331hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3857618
hg1957618
hg1857618
hg1757618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv391n27
Supporting Variantsnssv535247
Samples1780862093_A
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)nsv458284
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer