A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv459540



Internal ID15519605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:140671182..140730328hg38UCSC Ensembl
Innerchr2:141428751..141487897hg19UCSC Ensembl
Innerchr2:141145221..141204367hg18UCSC Ensembl
Innerchr2:141262483..141321629hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3859147
hg1959147
hg1859147
hg1759147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv477n27
Supporting Variantsnssv536275
SamplesNINDS_212
Known GenesLRP1B
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)nsv459540
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