A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv533666



Internal ID15156762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63312034..63385459hg38UCSC Ensembl
Innerchr14:63778748..63852177hg19UCSC Ensembl
Innerchr14:62848501..62921930hg18UCSC Ensembl
Innerchr14:62848501..62921930hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3873426
hg1973430
hg1873430
hg1773430
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv456325
Supporting Variants
Samples1780862274_A
Known GenesGPHB5, PPP2R5E
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)nssv533666
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