A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591850



Internal ID16379259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136490708..136581890hg38UCSC Ensembl
Innerchr3:136209550..136300732hg19UCSC Ensembl
Innerchr3:137692240..137783422hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3891183
hg1991183
hg1891183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974768
Samples
Known GenesSTAG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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