A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466296



Internal ID15526361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21122682..21130178hg38UCSC Ensembl
Innerchr9:21122681..21130177hg19UCSC Ensembl
Innerchr9:21112681..21120177hg18UCSC Ensembl
Innerchr9:21112681..21120177hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387497
hg197497
hg187497
hg177497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv541881
Samples1782681262_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)nsv466296
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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