A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466336



Internal ID15526401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27196121..27292705hg38UCSC Ensembl
Innerchr9:27196119..27292703hg19UCSC Ensembl
Innerchr9:27186119..27282703hg18UCSC Ensembl
Innerchr9:27186119..27282703hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3896585
hg1996585
hg1896585
hg1796585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv541908
SamplesHGDP01418
Known GenesEQTN, LINC00032, TEK
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)nsv466336
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