A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv460296



Internal ID15520361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31065..140991hg38UCSC Ensembl
Innerchr3:72739..182674hg19UCSC Ensembl
Innerchr3:47739..157674hg18UCSC Ensembl
Innerchr3:47739..157674hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38109927
hg19109936
hg18109936
hg17109936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv584n27
Supporting Variantsnssv536897
SamplesHGDP00096
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)nsv460296
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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