A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv457225



Internal ID15170604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85566351hg38UCSC Ensembl
Innerchr15:85825567..86109582hg19UCSC Ensembl
Innerchr15:83626571..83910586hg18UCSC Ensembl
Innerchr15:83626571..83910586hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38284016
hg19284016
hg18284016
hg17284016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv323n27
Supporting Variantsnssv534459
Samples1798860114_A
Known GenesAKAP13
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)nsv457225
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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