A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466267



Internal ID15526332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16937554..16982586hg38UCSC Ensembl
Innerchr9:16937552..16982584hg19UCSC Ensembl
Innerchr9:16927552..16972584hg18UCSC Ensembl
Innerchr9:16927552..16972584hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845033
hg1945033
hg1845033
hg1745033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv541860
Samples1782681313_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)nsv466267
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