A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466614



Internal ID15179993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133161872..133320327hg38UCSC Ensembl
Innerchr9:136037259..136187163hg19UCSC Ensembl
Innerchr9:135027080..135176984hg18UCSC Ensembl
Innerchr9:133066813..133216717hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38158456
hg19149905
hg18149905
hg17149905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv951n27
Supporting Variantsnssv542116
SamplesHGDP00547
Known GenesABO, GBGT1, OBP2B
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)nsv466614
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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